Canonical Allele Identifier: CA383457849

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750648T>G (hg19) ; chr11:g.130880753T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880753T>G , CM000673.2:g.130880753T>G	GRCh38
NC_000011.9:g.130750648T>G , CM000673.1:g.130750648T>G	GRCh37
NC_000011.8:g.130255858T>G	NCBI36
NG_053190.1:g.40736A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265909.9:c.2627A>C MANE Select	ENSP00000265909.4:p.Tyr876Ser
ENST00000265909.8:c.2627A>C	ENSP00000265909.4:p.Tyr876Ser
ENST00000426933.6:c.131A>C	ENSP00000413345.2:p.Tyr44Ser
ENST00000526579.5:n.178-1042A>C
ENST00000527116.5:n.389A>C
ENST00000528555.5:c.767A>C	ENSP00000435122.1:p.Tyr256Ser
ENST00000530330.1:n.363A>C
ENST00000530356.5:c.767A>C	ENSP00000432307.1:p.Tyr256Ser
ENST00000533318.5:n.987A>C
ENST00000534726.5:c.347A>C	ENSP00000433699.1:p.Tyr116Ser
NM_001301089.1:c.767A>C	NP_001288018.1:p.Tyr256Ser
NM_014758.2:c.2627A>C	NP_055573.2:p.Tyr876Ser
XM_005271546.3:c.2574-1042A>C	XP_005271603.1:n.2574-1042A>C
XM_011542819.1:c.2873A>C	XP_011541121.1:p.Tyr958Ser
XM_011542820.1:c.2861A>C	XP_011541122.1:p.Tyr954Ser
XM_011542821.1:c.2753A>C	XP_011541123.1:p.Tyr918Ser
XM_011542824.1:c.1991A>C	XP_011541126.1:p.Tyr664Ser
XM_011542825.1:c.1148A>C	XP_011541127.1:p.Tyr383Ser
XM_011542826.1:c.1013A>C	XP_011541128.1:p.Tyr338Ser
XM_011542827.1:c.893A>C	XP_011541129.1:p.Tyr298Ser
NM_001347918.1:c.2507A>C	NP_001334847.1:p.Tyr836Ser
NM_001347919.1:c.2574-1042A>C	NP_001334848.1:n.2574-1042A>C
NM_001347922.1:c.956A>C	NP_001334851.1:p.Tyr319Ser
NM_001347923.1:c.902A>C	NP_001334852.1:p.Tyr301Ser
NM_001347924.1:c.647A>C	NP_001334853.1:p.Tyr216Ser
NM_001347925.1:c.593A>C	NP_001334854.1:p.Tyr198Ser
NM_001347926.1:c.714-1042A>C	NP_001334855.1:n.714-1042A>C
NM_001347927.1:c.347A>C	NP_001334856.1:p.Tyr116Ser
NR_144939.1:n.3260A>C
XM_011542820.2:c.2861A>C	XP_011541122.1:p.Tyr954Ser
XM_011542821.3:c.2753A>C	XP_011541123.1:p.Tyr918Ser
XM_011542824.2:c.1991A>C	XP_011541126.1:p.Tyr664Ser
XM_011542825.2:c.1148A>C	XP_011541127.1:p.Tyr383Ser
XM_011542826.2:c.1013A>C	XP_011541128.1:p.Tyr338Ser
XM_024448521.1:c.2873A>C	XP_024304289.1:p.Tyr958Ser
XR_001747870.1:n.3698A>C
XR_001747872.1:n.3044A>C
XR_001747873.1:n.3358A>C
NM_001301089.2:c.767A>C	NP_001288018.1:p.Tyr256Ser
NM_001347918.2:c.2507A>C	NP_001334847.2:p.Tyr836Ser
NM_001347919.2:c.2574-1042A>C	NP_001334848.2:n.2574-1042A>C
NM_001347920.2:c.*21023A>C	NP_001334849.2:n.*21023A>C
NM_001347922.2:c.956A>C	NP_001334851.2:p.Tyr319Ser
NM_001347923.2:c.902A>C	NP_001334852.2:p.Tyr301Ser
NM_001347924.2:c.647A>C	NP_001334853.1:p.Tyr216Ser
NM_001347925.2:c.593A>C	NP_001334854.1:p.Tyr198Ser
NM_001347926.2:c.714-1042A>C	NP_001334855.1:n.714-1042A>C
NM_001347927.2:c.347A>C	NP_001334856.1:p.Tyr116Ser
NM_014758.3:c.2627A>C MANE Select	NP_055573.3:p.Tyr876Ser
NR_144939.2:n.3252A>C