Canonical Allele Identifier: CA8061699

Gene: SLC6A2

Linked Data

• dbSNP Id: rs201586185
• ExAC: 16:55730230 C / T
• gnomAD v2: 16-55730230-C-T
• gnomAD v3: 16-55696318-C-T
• gnomAD v4: 16-55696318-C-T
• COSMIC: COSM4970876 ; COSM4970877
• MyVariant Identifiers: chr16:g.55730230C>T (hg19) ; chr16:g.55696318C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55696318C>T , CM000678.2:g.55696318C>T	GRCh38
NC_000016.9:g.55730230C>T , CM000678.1:g.55730230C>T	GRCh37
NC_000016.8:g.54287731C>T	NCBI36
NG_016969.1:g.45689C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219833.13:c.1241C>T	ENSP00000219833.8:p.Ala414Val
ENST00000568943.6:c.1241C>T MANE Select	ENSP00000457473.1:p.Ala414Val
ENST00000574918.2:c.1106C>T	ENSP00000460214.2:p.Ala369Val
ENST00000682050.1:c.1012+916C>T	ENSP00000508367.1:n.1012+916C>T
ENST00000219833.12:c.1241C>T	ENSP00000219833.8:p.Ala414Val
ENST00000379906.6:c.1241C>T	ENSP00000369237.2:p.Ala414Val
ENST00000414754.7:c.1241C>T	ENSP00000394956.3:p.Ala414Val
ENST00000561820.5:c.1241C>T	ENSP00000454439.1:p.Ala414Val
ENST00000566163.5:c.1106C>T	ENSP00000456210.1:p.Ala369Val
ENST00000567238.1:c.926C>T	ENSP00000457375.1:p.Ala309Val
ENST00000568943.5:c.1241C>T	ENSP00000457473.1:p.Ala414Val
NM_001043.3:c.1241C>T	NP_001034.1:p.Ala414Val
NM_001172501.1:c.1241C>T	NP_001165972.1:p.Ala414Val
NM_001172502.1:c.926C>T	NP_001165973.1:p.Ala309Val
NM_001172504.1:c.1241C>T	NP_001165975.1:p.Ala414Val
XM_006721263.2:c.1241C>T	XP_006721326.1:p.Ala414Val
XM_011523295.1:c.1241C>T	XP_011521597.1:p.Ala414Val
XM_011523296.1:c.1106C>T	XP_011521598.1:p.Ala369Val
XM_011523297.1:c.1106C>T	XP_011521599.1:p.Ala369Val
XM_011523298.1:c.1147+916C>T	XP_011521600.1:n.1147+916C>T
XM_011523299.1:c.518C>T	XP_011521601.1:p.Ala173Val
XM_011523300.1:c.518C>T	XP_011521602.1:p.Ala173Val
XR_933403.1:n.1858C>T
XM_011523295.2:c.1241C>T	XP_011521597.1:p.Ala414Val
XM_011523296.2:c.1106C>T	XP_011521598.1:p.Ala369Val
XM_011523297.3:c.1106C>T	XP_011521599.1:p.Ala369Val
XM_011523298.2:c.1147+916C>T	XP_011521600.1:n.1147+916C>T
XM_011523299.2:c.518C>T	XP_011521601.1:p.Ala173Val
XM_011523300.2:c.518C>T	XP_011521602.1:p.Ala173Val
XR_933403.3:n.1534C>T
NM_001172501.2:c.1241C>T	NP_001165972.1:p.Ala414Val
NM_001172501.3:c.1241C>T MANE Select	NP_001165972.1:p.Ala414Val