Canonical Allele Identifier: CA2223789906

Gene: SLC6A2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55656400G= , CM000678.2:g.55656400G=	GRCh38
NC_000016.9:g.55690312G= , CM000678.1:g.55690312G=	GRCh37
NC_000016.8:g.54247813G=	NCBI36
NG_016969.1:g.5771G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000219833.13:c.-295G=	ENSP00000219833.8:n.-295G=
ENST00000568943.6:c.-52+231G= MANE Select	ENSP00000457473.1:n.-52+231G=
ENST00000574918.2:c.-52+48G=	ENSP00000460214.2:n.-52+48G=
ENST00000682050.1:c.-52+48G=	ENSP00000508367.1:n.-52+48G=
ENST00000414754.7:c.-52+231G=	ENSP00000394956.3:n.-52+231G=
ENST00000568529.6:c.-52+231G=	ENSP00000456377.2:n.-52+231G=
ENST00000568655.5:c.-52+48G=	ENSP00000454603.1:n.-52+48G=
ENST00000568943.5:c.-52+231G=	ENSP00000457473.1:n.-52+231G=
NM_001172501.1:c.-52+231G=	NP_001165972.1:n.-52+231G=
XM_006721263.2:c.-52+48G=	XP_006721326.1:n.-52+48G=
XM_011523295.1:c.-52+231G=	XP_011521597.1:n.-52+231G=
XM_011523296.1:c.-52+231G=	XP_011521598.1:n.-52+231G=
XM_011523297.1:c.-52+231G=	XP_011521599.1:n.-52+231G=
XM_011523298.1:c.-52+231G=	XP_011521600.1:n.-52+231G=
XR_933403.1:n.566+231G=
XM_011523295.2:c.-52+231G=	XP_011521597.1:n.-52+231G=
XM_011523296.2:c.-52+231G=	XP_011521598.1:n.-52+231G=
XM_011523297.3:c.-52+231G=	XP_011521599.1:n.-52+231G=
XM_011523298.2:c.-52+231G=	XP_011521600.1:n.-52+231G=
XR_933403.3:n.242+231G=
NM_001172501.2:c.-52+231G=	NP_001165972.1:n.-52+231G=
NM_001172501.3:c.-52+231G= MANE Select	NP_001165972.1:n.-52+231G=