Canonical Allele Identifier: CA2223789768

Gene: SLC6A2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55656146A= , CM000678.2:g.55656146A=	GRCh38
NC_000016.9:g.55690058A= , CM000678.1:g.55690058A=	GRCh37
NC_000016.8:g.54247559A=	NCBI36
NG_016969.1:g.5517A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000568943.6:c.-75A= MANE Select	ENSP00000457473.1:n.-75A=
ENST00000414754.7:c.-75A=	ENSP00000394956.3:n.-75A=
ENST00000568529.6:c.-75A=	ENSP00000456377.2:n.-75A=
ENST00000568943.5:c.-75A=	ENSP00000457473.1:n.-75A=
NM_001172501.1:c.-75A=	NP_001165972.1:n.-75A=
XM_011523295.1:c.-75A=	XP_011521597.1:n.-75A=
XM_011523296.1:c.-75A=	XP_011521598.1:n.-75A=
XM_011523297.1:c.-75A=	XP_011521599.1:n.-75A=
XM_011523298.1:c.-75A=	XP_011521600.1:n.-75A=
XR_933403.1:n.543A=
XM_011523295.2:c.-75A=	XP_011521597.1:n.-75A=
XM_011523296.2:c.-75A=	XP_011521598.1:n.-75A=
XM_011523297.3:c.-75A=	XP_011521599.1:n.-75A=
XM_011523298.2:c.-75A=	XP_011521600.1:n.-75A=
XR_933403.3:n.219A=
NM_001172501.2:c.-75A=	NP_001165972.1:n.-75A=
NM_001172501.3:c.-75A= MANE Select	NP_001165972.1:n.-75A=