Canonical Allele Identifier: CA2807127269

Gene: SLC6A2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55696391_55696392del , CM000678.2:g.55696391_55696392del	GRCh38
NC_000016.9:g.55730303_55730304del , CM000678.1:g.55730303_55730304del	GRCh37
NC_000016.8:g.54287804_54287805del	NCBI36
NG_016969.1:g.45762_45763del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219833.13:c.1260+54_1260+55del	ENSP00000219833.8:n.1260+54_1260+55del
ENST00000568943.6:c.1260+54_1260+55del MANE Select	ENSP00000457473.1:n.1260+54_1260+55del
ENST00000574918.2:c.1125+54_1125+55del	ENSP00000460214.2:n.1125+54_1125+55del
ENST00000682050.1:c.1012+989_1012+990del	ENSP00000508367.1:n.1012+989_1012+990del
ENST00000219833.12:c.1260+54_1260+55del	ENSP00000219833.8:n.1260+54_1260+55del
ENST00000379906.6:c.1260+54_1260+55del	ENSP00000369237.2:n.1260+54_1260+55del
ENST00000414754.7:c.1260+54_1260+55del	ENSP00000394956.3:n.1260+54_1260+55del
ENST00000561820.5:c.1260+54_1260+55del	ENSP00000454439.1:n.1260+54_1260+55del
ENST00000566163.5:c.1125+54_1125+55del	ENSP00000456210.1:n.1125+54_1125+55del
ENST00000567238.1:c.945+54_945+55del	ENSP00000457375.1:n.945+54_945+55del
ENST00000568943.5:c.1260+54_1260+55del	ENSP00000457473.1:n.1260+54_1260+55del
NM_001043.3:c.1260+54_1260+55del	NP_001034.1:n.1260+54_1260+55del
NM_001172501.1:c.1260+54_1260+55del	NP_001165972.1:n.1260+54_1260+55del
NM_001172502.1:c.945+54_945+55del	NP_001165973.1:n.945+54_945+55del
NM_001172504.1:c.1260+54_1260+55del	NP_001165975.1:n.1260+54_1260+55del
XM_006721263.2:c.1260+54_1260+55del	XP_006721326.1:n.1260+54_1260+55del
XM_011523295.1:c.1260+54_1260+55del	XP_011521597.1:n.1260+54_1260+55del
XM_011523296.1:c.1125+54_1125+55del	XP_011521598.1:n.1125+54_1125+55del
XM_011523297.1:c.1125+54_1125+55del	XP_011521599.1:n.1125+54_1125+55del
XM_011523298.1:c.1147+989_1147+990del	XP_011521600.1:n.1147+989_1147+990del
XM_011523299.1:c.537+54_537+55del	XP_011521601.1:n.537+54_537+55del
XM_011523300.1:c.537+54_537+55del	XP_011521602.1:n.537+54_537+55del
XR_933403.1:n.1877+54_1877+55del
XM_011523295.2:c.1260+54_1260+55del	XP_011521597.1:n.1260+54_1260+55del
XM_011523296.2:c.1125+54_1125+55del	XP_011521598.1:n.1125+54_1125+55del
XM_011523297.3:c.1125+54_1125+55del	XP_011521599.1:n.1125+54_1125+55del
XM_011523298.2:c.1147+989_1147+990del	XP_011521600.1:n.1147+989_1147+990del
XM_011523299.2:c.537+54_537+55del	XP_011521601.1:n.537+54_537+55del
XM_011523300.2:c.537+54_537+55del	XP_011521602.1:n.537+54_537+55del
XR_933403.3:n.1553+54_1553+55del
NM_001172501.2:c.1260+54_1260+55del	NP_001165972.1:n.1260+54_1260+55del
NM_001172501.3:c.1260+54_1260+55del MANE Select	NP_001165972.1:n.1260+54_1260+55del