Canonical Allele Identifier: CA1947288563

Gene: SLC25A22

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.792429G= , CM000673.2:g.792429G=	GRCh38
NC_000011.9:g.792429G= , CM000673.1:g.792429G=	GRCh37
NC_000011.8:g.782429G=	NCBI36
NG_023407.1:g.10841C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000628067.3:c.617C= MANE Select	ENSP00000486058.1:p.Pro206=
ENST00000320230.9:c.617C=	ENSP00000322020.5:p.Pro206=
ENST00000481290.5:c.692C=	ENSP00000431829.2:p.Pro231=
ENST00000531214.5:c.617C=	ENSP00000437236.1:p.Pro206=
ENST00000627843.2:c.617C=	ENSP00000486512.1:p.Pro206=
ENST00000628067.2:c.617C=	ENSP00000486058.1:p.Pro206=
ENST00000630809.2:n.485C=
NM_001191060.1:c.617C=	NP_001177989.1:p.Pro206=
NM_001191061.1:c.617C=	NP_001177990.1:p.Pro206=
NM_024698.5:c.617C=	NP_078974.1:p.Pro206=
XM_011520369.1:c.617C=	XP_011518671.1:p.Pro206=
XM_011520370.1:c.617C=	XP_011518672.1:p.Pro206=
XM_011520371.1:c.617C=	XP_011518673.1:p.Pro206=
XM_011520370.2:c.617C=	XP_011518672.1:p.Pro206=
XM_011520371.2:c.617C=	XP_011518673.1:p.Pro206=
XM_024448687.1:c.617C=	XP_024304455.1:p.Pro206=
XM_024448688.1:c.617C=	XP_024304456.1:p.Pro206=
XM_024448689.1:c.617C=	XP_024304457.1:p.Pro206=
NM_001191061.2:c.617C= MANE Select	NP_001177990.1:p.Pro206=
NM_024698.6:c.617C=	NP_078974.1:p.Pro206=
NM_001191060.2:c.617C=	NP_001177989.1:p.Pro206=