Canonical Allele Identifier: CA383457819

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750633T>G (hg19) ; chr11:g.130880738T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880738T>G , CM000673.2:g.130880738T>G	GRCh38
NC_000011.9:g.130750633T>G , CM000673.1:g.130750633T>G	GRCh37
NC_000011.8:g.130255843T>G	NCBI36
NG_053190.1:g.40751A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2642A>C MANE Select	ENSP00000265909.4:p.Gln881Pro
ENST00000265909.8:c.2642A>C	ENSP00000265909.4:p.Gln881Pro
ENST00000426933.6:c.146A>C	ENSP00000413345.2:p.Gln49Pro
ENST00000526579.5:n.178-1027A>C
ENST00000527116.5:n.404A>C
ENST00000528555.5:c.782A>C	ENSP00000435122.1:p.Gln261Pro
ENST00000530330.1:n.378A>C
ENST00000530356.5:c.782A>C	ENSP00000432307.1:p.Gln261Pro
ENST00000533318.5:n.1002A>C
ENST00000534726.5:c.362A>C	ENSP00000433699.1:p.Gln121Pro
NM_001301089.1:c.782A>C	NP_001288018.1:p.Gln261Pro
NM_014758.2:c.2642A>C	NP_055573.2:p.Gln881Pro
XM_005271546.3:c.2574-1027A>C	XP_005271603.1:n.2574-1027A>C
XM_011542819.1:c.2888A>C	XP_011541121.1:p.Gln963Pro
XM_011542820.1:c.2876A>C	XP_011541122.1:p.Gln959Pro
XM_011542821.1:c.2768A>C	XP_011541123.1:p.Gln923Pro
XM_011542824.1:c.2006A>C	XP_011541126.1:p.Gln669Pro
XM_011542825.1:c.1163A>C	XP_011541127.1:p.Gln388Pro
XM_011542826.1:c.1028A>C	XP_011541128.1:p.Gln343Pro
XM_011542827.1:c.908A>C	XP_011541129.1:p.Gln303Pro
NM_001347918.1:c.2522A>C	NP_001334847.1:p.Gln841Pro
NM_001347919.1:c.2574-1027A>C	NP_001334848.1:n.2574-1027A>C
NM_001347922.1:c.971A>C	NP_001334851.1:p.Gln324Pro
NM_001347923.1:c.917A>C	NP_001334852.1:p.Gln306Pro
NM_001347924.1:c.662A>C	NP_001334853.1:p.Gln221Pro
NM_001347925.1:c.608A>C	NP_001334854.1:p.Gln203Pro
NM_001347926.1:c.714-1027A>C	NP_001334855.1:n.714-1027A>C
NM_001347927.1:c.362A>C	NP_001334856.1:p.Gln121Pro
NR_144939.1:n.3275A>C
XM_011542820.2:c.2876A>C	XP_011541122.1:p.Gln959Pro
XM_011542821.3:c.2768A>C	XP_011541123.1:p.Gln923Pro
XM_011542824.2:c.2006A>C	XP_011541126.1:p.Gln669Pro
XM_011542825.2:c.1163A>C	XP_011541127.1:p.Gln388Pro
XM_011542826.2:c.1028A>C	XP_011541128.1:p.Gln343Pro
XM_024448521.1:c.2888A>C	XP_024304289.1:p.Gln963Pro
XR_001747870.1:n.3713A>C
XR_001747872.1:n.3059A>C
XR_001747873.1:n.3373A>C
NM_001301089.2:c.782A>C	NP_001288018.1:p.Gln261Pro
NM_001347918.2:c.2522A>C	NP_001334847.2:p.Gln841Pro
NM_001347919.2:c.2574-1027A>C	NP_001334848.2:n.2574-1027A>C
NM_001347920.2:c.*21038A>C	NP_001334849.2:n.*21038A>C
NM_001347922.2:c.971A>C	NP_001334851.2:p.Gln324Pro
NM_001347923.2:c.917A>C	NP_001334852.2:p.Gln306Pro
NM_001347924.2:c.662A>C	NP_001334853.1:p.Gln221Pro
NM_001347925.2:c.608A>C	NP_001334854.1:p.Gln203Pro
NM_001347926.2:c.714-1027A>C	NP_001334855.1:n.714-1027A>C
NM_001347927.2:c.362A>C	NP_001334856.1:p.Gln121Pro
NM_014758.3:c.2642A>C MANE Select	NP_055573.3:p.Gln881Pro
NR_144939.2:n.3267A>C