Canonical Allele Identifier: CA2223791769

Gene: SLC6A2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55661094_55661097delinsTATC , CM000678.2:g.55661094_55661097delinsTATC	GRCh38
NC_000016.9:g.55695006_55695009delinsTATC , CM000678.1:g.55695006_55695009delinsTATC	GRCh37
NC_000016.8:g.54252507_54252510delinsTATC	NCBI36
NG_016969.1:g.10465_10468delinsTATC

Transcript Alleles

HGVS	Amino-acid change
ENST00000219833.13:c.274+4126_274+4129delinsTATC	ENSP00000219833.8:n.274+4126_274+4129deli...
ENST00000568943.6:c.274+4126_274+4129delinsTATC MANE Select	ENSP00000457473.1:n.274+4126_274+4129deli...
ENST00000574918.2:c.274+4126_274+4129delinsTATC	ENSP00000460214.2:n.274+4126_274+4129deli...
ENST00000682050.1:c.274+4126_274+4129delinsTATC	ENSP00000508367.1:n.274+4126_274+4129deli...
ENST00000219833.12:c.274+4126_274+4129delinsTATC	ENSP00000219833.8:n.274+4126_274+4129deli...
ENST00000379906.6:c.274+4126_274+4129delinsTATC	ENSP00000369237.2:n.274+4126_274+4129deli...
ENST00000414754.7:c.274+4126_274+4129delinsTATC	ENSP00000394956.3:n.274+4126_274+4129deli...
ENST00000561820.5:c.274+4126_274+4129delinsTATC	ENSP00000454439.1:n.274+4126_274+4129deli...
ENST00000566163.5:c.274+4126_274+4129delinsTATC	ENSP00000456210.1:n.274+4126_274+4129deli...
ENST00000568529.6:c.274+4126_274+4129delinsTATC	ENSP00000456377.2:n.274+4126_274+4129deli...
ENST00000568655.5:c.274+4126_274+4129delinsTATC	ENSP00000454603.1:n.274+4126_274+4129deli...
ENST00000568943.5:c.274+4126_274+4129delinsTATC	ENSP00000457473.1:n.274+4126_274+4129deli...
NM_001043.3:c.274+4126_274+4129delinsTATC	NP_001034.1:n.274+4126_274+4129delinsTATC...
NM_001172501.1:c.274+4126_274+4129delinsTATC	NP_001165972.1:n.274+4126_274+4129delinsT...
NM_001172504.1:c.274+4126_274+4129delinsTATC	NP_001165975.1:n.274+4126_274+4129delinsT...
XM_006721263.2:c.274+4126_274+4129delinsTATC	XP_006721326.1:n.274+4126_274+4129delinsT...
XM_011523295.1:c.274+4126_274+4129delinsTATC	XP_011521597.1:n.274+4126_274+4129delinsT...
XM_011523296.1:c.274+4126_274+4129delinsTATC	XP_011521598.1:n.274+4126_274+4129delinsT...
XM_011523297.1:c.274+4126_274+4129delinsTATC	XP_011521599.1:n.274+4126_274+4129delinsT...
XM_011523298.1:c.274+4126_274+4129delinsTATC	XP_011521600.1:n.274+4126_274+4129delinsT...
XR_933403.1:n.891+4126_891+4129delinsTATC
XM_011523295.2:c.274+4126_274+4129delinsTATC	XP_011521597.1:n.274+4126_274+4129delinsT...
XM_011523296.2:c.274+4126_274+4129delinsTATC	XP_011521598.1:n.274+4126_274+4129delinsT...
XM_011523297.3:c.274+4126_274+4129delinsTATC	XP_011521599.1:n.274+4126_274+4129delinsT...
XM_011523298.2:c.274+4126_274+4129delinsTATC	XP_011521600.1:n.274+4126_274+4129delinsT...
XR_933403.3:n.567+4126_567+4129delinsTATC
NM_001172501.2:c.274+4126_274+4129delinsTATC	NP_001165972.1:n.274+4126_274+4129delinsT...
NM_001172501.3:c.274+4126_274+4129delinsTATC MANE Select	NP_001165972.1:n.274+4126_274+4129delinsT...