Canonical Allele Identifier: CA477582312

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750617A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880722A>G , CM000673.2:g.130880722A>G	GRCh38
NC_000011.9:g.130750617A>G , CM000673.1:g.130750617A>G	GRCh37
NC_000011.8:g.130255827A>G	NCBI36
NG_053190.1:g.40767T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2658T>C MANE Select	ENSP00000265909.4:p.Pro886=
ENST00000265909.8:c.2658T>C	ENSP00000265909.4:p.Pro886=
ENST00000426933.6:c.162T>C	ENSP00000413345.2:p.Pro54=
ENST00000526579.5:n.178-1011T>C
ENST00000527116.5:n.420T>C
ENST00000528555.5:c.798T>C	ENSP00000435122.1:p.Pro266=
ENST00000530330.1:n.394T>C
ENST00000530356.5:c.798T>C	ENSP00000432307.1:p.Pro266=
ENST00000533318.5:n.1018T>C
ENST00000534726.5:c.378T>C	ENSP00000433699.1:p.Pro126=
NM_001301089.1:c.798T>C	NP_001288018.1:p.Pro266=
NM_014758.2:c.2658T>C	NP_055573.2:p.Pro886=
XM_005271546.3:c.2574-1011T>C	XP_005271603.1:n.2574-1011T>C
XM_011542819.1:c.2904T>C	XP_011541121.1:p.Pro968=
XM_011542820.1:c.2892T>C	XP_011541122.1:p.Pro964=
XM_011542821.1:c.2784T>C	XP_011541123.1:p.Pro928=
XM_011542824.1:c.2022T>C	XP_011541126.1:p.Pro674=
XM_011542825.1:c.1179T>C	XP_011541127.1:p.Pro393=
XM_011542826.1:c.1044T>C	XP_011541128.1:p.Pro348=
XM_011542827.1:c.924T>C	XP_011541129.1:p.Pro308=
NM_001347918.1:c.2538T>C	NP_001334847.1:p.Pro846=
NM_001347919.1:c.2574-1011T>C	NP_001334848.1:n.2574-1011T>C
NM_001347922.1:c.987T>C	NP_001334851.1:p.Pro329=
NM_001347923.1:c.933T>C	NP_001334852.1:p.Pro311=
NM_001347924.1:c.678T>C	NP_001334853.1:p.Pro226=
NM_001347925.1:c.624T>C	NP_001334854.1:p.Pro208=
NM_001347926.1:c.714-1011T>C	NP_001334855.1:n.714-1011T>C
NM_001347927.1:c.378T>C	NP_001334856.1:p.Pro126=
NR_144939.1:n.3291T>C
XM_011542820.2:c.2892T>C	XP_011541122.1:p.Pro964=
XM_011542821.3:c.2784T>C	XP_011541123.1:p.Pro928=
XM_011542824.2:c.2022T>C	XP_011541126.1:p.Pro674=
XM_011542825.2:c.1179T>C	XP_011541127.1:p.Pro393=
XM_011542826.2:c.1044T>C	XP_011541128.1:p.Pro348=
XM_024448521.1:c.2904T>C	XP_024304289.1:p.Pro968=
XR_001747870.1:n.3729T>C
XR_001747872.1:n.3075T>C
XR_001747873.1:n.3389T>C
NM_001301089.2:c.798T>C	NP_001288018.1:p.Pro266=
NM_001347918.2:c.2538T>C	NP_001334847.2:p.Pro846=
NM_001347919.2:c.2574-1011T>C	NP_001334848.2:n.2574-1011T>C
NM_001347920.2:c.*21054T>C	NP_001334849.2:n.*21054T>C
NM_001347922.2:c.987T>C	NP_001334851.2:p.Pro329=
NM_001347923.2:c.933T>C	NP_001334852.2:p.Pro311=
NM_001347924.2:c.678T>C	NP_001334853.1:p.Pro226=
NM_001347925.2:c.624T>C	NP_001334854.1:p.Pro208=
NM_001347926.2:c.714-1011T>C	NP_001334855.1:n.714-1011T>C
NM_001347927.2:c.378T>C	NP_001334856.1:p.Pro126=
NM_014758.3:c.2658T>C MANE Select	NP_055573.3:p.Pro886=
NR_144939.2:n.3283T>C