Canonical Allele Identifier: CA514339647

Gene: RBFOX2

Linked Data

• MyVariant Identifiers: chr22:g.36157298T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35761251T>G , CM000684.2:g.35761251T>G	GRCh38
NC_000022.10:g.36157298T>G , CM000684.1:g.36157298T>G	GRCh37
NC_000022.9:g.34487244T>G	NCBI36
NG_029628.1:g.272288A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000695803.1:c.825A>C	ENSP00000512183.1:p.Ala275=
ENST00000695804.1:c.705A>C	ENSP00000512184.1:p.Ala235=
ENST00000695805.1:c.*236A>C	ENSP00000512185.1:n.*236A>C
ENST00000695806.1:c.*212A>C	ENSP00000512186.1:n.*212A>C
ENST00000695807.1:c.*155A>C	ENSP00000512187.1:n.*155A>C
ENST00000695854.1:c.915A>C MANE Select	ENSP00000512219.1:p.Ala305=
ENST00000438146.7:c.915A>C	ENSP00000413035.2:p.Ala305=
ENST00000262829.11:c.648A>C	ENSP00000262829.7:p.Ala216=
ENST00000359369.8:c.642A>C	ENSP00000352328.4:p.Ala214=
ENST00000397303.6:c.645A>C	ENSP00000380470.2:p.Ala215=
ENST00000405409.6:c.705A>C	ENSP00000384944.2:p.Ala235=
ENST00000414461.6:c.702A>C	ENSP00000407855.2:p.Ala234=
ENST00000416721.6:c.702A>C	ENSP00000405651.2:p.Ala234=
ENST00000438146.6:c.915A>C	ENSP00000413035.2:p.Ala305=
ENST00000449924.6:c.702A>C	ENSP00000391670.2:p.Ala234=
ENST00000473487.6:c.642A>C	ENSP00000475142.1:p.Ala214=
ENST00000495377.6:c.260A>C
NM_001031695.2:c.702A>C	NP_001026865.1:p.Ala234=
NM_001082576.1:c.702A>C	NP_001076045.1:p.Ala234=
NM_001082577.1:c.702A>C	NP_001076046.1:p.Ala234=
NM_001082578.1:c.915A>C	NP_001076047.1:p.Ala305=
NM_001082579.1:c.912A>C	NP_001076048.1:p.Ala304=
NM_014309.2:c.705A>C	NP_055124.1:p.Ala235=
XM_005261428.2:c.915A>C	XP_005261485.1:p.Ala305=
XM_005261429.2:c.912A>C	XP_005261486.1:p.Ala304=
XM_005261430.2:c.915A>C	XP_005261487.1:p.Ala305=
XM_005261431.2:c.915A>C	XP_005261488.1:p.Ala305=
XM_005261432.2:c.912A>C	XP_005261489.1:p.Ala304=
XM_005261433.2:c.915A>C	XP_005261490.1:p.Ala305=
XM_005261435.1:c.702A>C	XP_005261492.1:p.Ala234=
XM_005261437.1:c.705A>C	XP_005261494.1:p.Ala235=
XM_006724185.2:c.915A>C	XP_006724248.1:p.Ala305=
XM_006724186.2:c.912A>C	XP_006724249.1:p.Ala304=
XM_006724187.2:c.915A>C	XP_006724250.1:p.Ala305=
XM_006724188.2:c.915A>C	XP_006724251.1:p.Ala305=
XM_006724189.2:c.771A>C	XP_006724252.1:p.Ala257=
XM_006724190.1:c.768A>C	XP_006724253.1:p.Ala256=
XM_006724191.1:c.705A>C	XP_006724254.1:p.Ala235=
XM_006724192.2:c.693A>C	XP_006724255.1:p.Ala231=
XM_006724193.2:c.915A>C	XP_006724256.1:p.Ala305=
XM_006724194.1:c.642A>C	XP_006724257.1:p.Ala214=
XM_011530036.1:c.741A>C	XP_011528338.1:p.Ala247=
NM_001031695.3:c.702A>C	NP_001026865.1:p.Ala234=
NM_001082576.2:c.702A>C	NP_001076045.1:p.Ala234=
NM_001082577.2:c.702A>C	NP_001076046.1:p.Ala234=
NM_001082578.2:c.915A>C	NP_001076047.1:p.Ala305=
NM_001082579.2:c.912A>C	NP_001076048.1:p.Ala304=
NM_001349982.1:c.768A>C	NP_001336911.1:p.Ala256=
NM_001349983.1:c.702A>C	NP_001336912.1:p.Ala234=
NM_001349989.1:c.768A>C	NP_001336918.1:p.Ala256=
NM_001349990.1:c.768A>C	NP_001336919.1:p.Ala256=
NM_001349991.1:c.768A>C	NP_001336920.1:p.Ala256=
NM_001349992.1:c.768A>C	NP_001336921.1:p.Ala256=
NM_001349994.1:c.768A>C	NP_001336923.1:p.Ala256=
NM_001349995.1:c.675A>C	NP_001336924.1:p.Ala225=
NM_001349996.1:c.768A>C	NP_001336925.1:p.Ala256=
NM_001349997.1:c.705A>C	NP_001336926.1:p.Ala235=
NM_001349998.1:c.702A>C	NP_001336927.1:p.Ala234=
NM_001349999.1:c.915A>C	NP_001336928.1:p.Ala305=
NM_014309.3:c.705A>C	NP_055124.1:p.Ala235=
XM_006724189.3:c.771A>C	XP_006724252.1:p.Ala257=
XM_006724193.3:c.915A>C	XP_006724256.1:p.Ala305=
XM_006724194.2:c.642A>C	XP_006724257.1:p.Ala214=
XM_017028686.1:c.741A>C	XP_016884175.1:p.Ala247=
XM_017028687.2:c.837A>C	XP_016884176.1:p.Ala279=
XM_017028688.1:c.912A>C	XP_016884177.1:p.Ala304=
XM_017028690.1:c.723A>C	XP_016884179.1:p.Ala241=
XM_017028691.1:c.720A>C	XP_016884180.1:p.Ala240=
XM_017028693.1:c.705A>C	XP_016884182.1:p.Ala235=
XM_017028696.1:c.705A>C	XP_016884185.1:p.Ala235=
XM_017028697.1:c.642A>C	XP_016884186.1:p.Ala214=
XM_017028698.1:c.702A>C	XP_016884187.1:p.Ala234=
XM_024452188.1:c.834A>C	XP_024307956.1:p.Ala278=
XM_024452189.1:c.645A>C	XP_024307957.1:p.Ala215=
XM_024452190.1:c.645A>C	XP_024307958.1:p.Ala215=
XM_024452191.1:c.690A>C	XP_024307959.1:p.Ala230=
XM_024452192.1:c.642A>C	XP_024307960.1:p.Ala214=
NM_001082578.3:c.915A>C	NP_001076047.1:p.Ala305=
NM_001031695.4:c.702A>C	NP_001026865.1:p.Ala234=
NM_001082576.3:c.702A>C	NP_001076045.1:p.Ala234=
NM_001082577.3:c.702A>C	NP_001076046.1:p.Ala234=
NM_001349982.2:c.768A>C	NP_001336911.1:p.Ala256=
NM_001349983.2:c.702A>C	NP_001336912.1:p.Ala234=
NM_001349989.2:c.768A>C	NP_001336918.1:p.Ala256=
NM_001349990.2:c.768A>C	NP_001336919.1:p.Ala256=
NM_001349991.2:c.768A>C	NP_001336920.1:p.Ala256=
NM_001349992.2:c.768A>C	NP_001336921.1:p.Ala256=
NM_001349994.2:c.768A>C	NP_001336923.1:p.Ala256=
NM_001349995.2:c.675A>C	NP_001336924.1:p.Ala225=
NM_001349996.2:c.768A>C	NP_001336925.1:p.Ala256=
NM_001349997.2:c.705A>C	NP_001336926.1:p.Ala235=
NM_001349998.2:c.702A>C	NP_001336927.1:p.Ala234=
NM_014309.4:c.705A>C	NP_055124.1:p.Ala235=
NM_001082578.4:c.915A>C	NP_001076047.2:p.Ala305=
NM_001082579.3:c.912A>C	NP_001076048.2:p.Ala304=
NM_001349999.2:c.915A>C MANE Select	NP_001336928.2:p.Ala305=
NM_001394108.1:c.909A>C	NP_001381037.1:p.Ala303=
NM_001394109.1:c.819A>C	NP_001381038.1:p.Ala273=
NM_001394110.1:c.819A>C	NP_001381039.1:p.Ala273=
NM_001394111.1:c.819A>C	NP_001381040.1:p.Ala273=
NM_001394112.1:c.912A>C	NP_001381041.1:p.Ala304=
NM_001394113.1:c.912A>C	NP_001381042.1:p.Ala304=
NM_001394114.1:c.915A>C	NP_001381043.1:p.Ala305=
NM_001394115.1:c.912A>C	NP_001381044.1:p.Ala304=