Canonical Allele Identifier: CA977584946

Gene: SLC6A2

Linked Data

• dbSNP Id: rs1965779715
• gnomAD v3: 16-55695804-C-CAATAGTATTCACACCCCAATCAATCCAGCTCTGGAGCTTGTGTCCTTCCCTGCAGCT
• gnomAD v4: 16-55695804-C-CAATAGTATTCACACCCCAATCAATCCAGCTCTGGAGCTTGTGTCCTTCCCTGCAGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55695805_55695861dup , CM000678.2:g.55695805_55695861dup	GRCh38
NC_000016.9:g.55729717_55729773dup , CM000678.1:g.55729717_55729773dup	GRCh37
NC_000016.8:g.54287218_54287274dup	NCBI36
NG_016969.1:g.45176_45232dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000219833.13:c.1147+403_1148-364dup	ENSP00000219833.8:n.1147+403_1148-364dup
ENST00000568943.6:c.1147+403_1148-364dup MANE Select	ENSP00000457473.1:n.1147+403_1148-364dup
ENST00000574918.2:c.1012+403_1013-364dup	ENSP00000460214.2:n.1012+403_1013-364dup
ENST00000682050.1:c.1012+403_1012+459dup	ENSP00000508367.1:n.1012+403_1012+459dup
ENST00000219833.12:c.1147+403_1148-364dup	ENSP00000219833.8:n.1147+403_1148-364dup
ENST00000379906.6:c.1147+403_1148-364dup	ENSP00000369237.2:n.1147+403_1148-364dup
ENST00000414754.7:c.1147+403_1148-364dup	ENSP00000394956.3:n.1147+403_1148-364dup
ENST00000561820.5:c.1147+403_1148-364dup	ENSP00000454439.1:n.1147+403_1148-364dup
ENST00000566163.5:c.1012+403_1013-364dup	ENSP00000456210.1:n.1012+403_1013-364dup
ENST00000567238.1:c.832+403_833-364dup	ENSP00000457375.1:n.832+403_833-364dup
ENST00000568943.5:c.1147+403_1148-364dup	ENSP00000457473.1:n.1147+403_1148-364dup
NM_001043.3:c.1147+403_1148-364dup	NP_001034.1:n.1147+403_1148-364dup
NM_001172501.1:c.1147+403_1148-364dup	NP_001165972.1:n.1147+403_1148-364dup
NM_001172502.1:c.832+403_833-364dup	NP_001165973.1:n.832+403_833-364dup
NM_001172504.1:c.1147+403_1148-364dup	NP_001165975.1:n.1147+403_1148-364dup
XM_006721263.2:c.1147+403_1148-364dup	XP_006721326.1:n.1147+403_1148-364dup
XM_011523295.1:c.1147+403_1148-364dup	XP_011521597.1:n.1147+403_1148-364dup
XM_011523296.1:c.1012+403_1013-364dup	XP_011521598.1:n.1012+403_1013-364dup
XM_011523297.1:c.1012+403_1013-364dup	XP_011521599.1:n.1012+403_1013-364dup
XM_011523298.1:c.1147+403_1147+459dup	XP_011521600.1:n.1147+403_1147+459dup
XM_011523299.1:c.424+403_425-364dup	XP_011521601.1:n.424+403_425-364dup
XM_011523300.1:c.424+403_425-364dup	XP_011521602.1:n.424+403_425-364dup
XR_933403.1:n.1764+403_1765-364dup
XM_011523295.2:c.1147+403_1148-364dup	XP_011521597.1:n.1147+403_1148-364dup
XM_011523296.2:c.1012+403_1013-364dup	XP_011521598.1:n.1012+403_1013-364dup
XM_011523297.3:c.1012+403_1013-364dup	XP_011521599.1:n.1012+403_1013-364dup
XM_011523298.2:c.1147+403_1147+459dup	XP_011521600.1:n.1147+403_1147+459dup
XM_011523299.2:c.424+403_425-364dup	XP_011521601.1:n.424+403_425-364dup
XM_011523300.2:c.424+403_425-364dup	XP_011521602.1:n.424+403_425-364dup
XR_933403.3:n.1440+403_1441-364dup
NM_001172501.2:c.1147+403_1148-364dup	NP_001165972.1:n.1147+403_1148-364dup
NM_001172501.3:c.1147+403_1148-364dup MANE Select	NP_001165972.1:n.1147+403_1148-364dup