Canonical Allele Identifier: CA2223806513

Gene: SLC6A2

Linked Data

• dbSNP Id: rs1965838461

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55697624_55697627del , CM000678.2:g.55697624_55697627del	GRCh38
NC_000016.9:g.55731536_55731539del , CM000678.1:g.55731536_55731539del	GRCh37
NC_000016.8:g.54289037_54289040del	NCBI36
NG_016969.1:g.46995_46998del

Transcript Alleles

HGVS	Amino-acid change
ENST00000219833.13:c.1261-273_1261-270del	ENSP00000219833.8:n.1261-273_1261-270del
ENST00000568943.6:c.1261-273_1261-270del MANE Select	ENSP00000457473.1:n.1261-273_1261-270del
ENST00000574918.2:c.1126-273_1126-270del	ENSP00000460214.2:n.1126-273_1126-270del
ENST00000682050.1:c.1013-273_1013-270del	ENSP00000508367.1:n.1013-273_1013-270del
ENST00000219833.12:c.1261-273_1261-270del	ENSP00000219833.8:n.1261-273_1261-270del
ENST00000379906.6:c.1261-273_1261-270del	ENSP00000369237.2:n.1261-273_1261-270del
ENST00000414754.7:c.1261-273_1261-270del	ENSP00000394956.3:n.1261-273_1261-270del
ENST00000561820.5:c.1261-273_1261-270del	ENSP00000454439.1:n.1261-273_1261-270del
ENST00000566163.5:c.1126-273_1126-270del	ENSP00000456210.1:n.1126-273_1126-270del
ENST00000567238.1:c.946-273_946-270del	ENSP00000457375.1:n.946-273_946-270del
ENST00000568943.5:c.1261-273_1261-270del	ENSP00000457473.1:n.1261-273_1261-270del
NM_001043.3:c.1261-273_1261-270del	NP_001034.1:n.1261-273_1261-270del
NM_001172501.1:c.1261-273_1261-270del	NP_001165972.1:n.1261-273_1261-270del
NM_001172502.1:c.946-273_946-270del	NP_001165973.1:n.946-273_946-270del
NM_001172504.1:c.1261-273_1261-270del	NP_001165975.1:n.1261-273_1261-270del
XM_006721263.2:c.1261-273_1261-270del	XP_006721326.1:n.1261-273_1261-270del
XM_011523295.1:c.1261-273_1261-270del	XP_011521597.1:n.1261-273_1261-270del
XM_011523296.1:c.1126-273_1126-270del	XP_011521598.1:n.1126-273_1126-270del
XM_011523297.1:c.1126-273_1126-270del	XP_011521599.1:n.1126-273_1126-270del
XM_011523298.1:c.1148-273_1148-270del	XP_011521600.1:n.1148-273_1148-270del
XM_011523299.1:c.538-273_538-270del	XP_011521601.1:n.538-273_538-270del
XM_011523300.1:c.538-273_538-270del	XP_011521602.1:n.538-273_538-270del
XR_933403.1:n.1878-273_1878-270del
XM_011523295.2:c.1261-273_1261-270del	XP_011521597.1:n.1261-273_1261-270del
XM_011523296.2:c.1126-273_1126-270del	XP_011521598.1:n.1126-273_1126-270del
XM_011523297.3:c.1126-273_1126-270del	XP_011521599.1:n.1126-273_1126-270del
XM_011523298.2:c.1148-273_1148-270del	XP_011521600.1:n.1148-273_1148-270del
XM_011523299.2:c.538-273_538-270del	XP_011521601.1:n.538-273_538-270del
XM_011523300.2:c.538-273_538-270del	XP_011521602.1:n.538-273_538-270del
XR_933403.3:n.1554-273_1554-270del
NM_001172501.2:c.1261-273_1261-270del	NP_001165972.1:n.1261-273_1261-270del
NM_001172501.3:c.1261-273_1261-270del MANE Select	NP_001165972.1:n.1261-273_1261-270del