Canonical Allele Identifier: CA395947378

Gene: SLC6A2

Linked Data

• MyVariant Identifiers: chr16:g.55733469T>C (hg19) ; chr16:g.55699557T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55699557T>C , CM000678.2:g.55699557T>C	GRCh38
NC_000016.9:g.55733469T>C , CM000678.1:g.55733469T>C	GRCh37
NC_000016.8:g.54290970T>C	NCBI36
NG_016969.1:g.48928T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000219833.13:c.1493T>C	ENSP00000219833.8:p.Val498Ala
ENST00000568943.6:c.1493T>C MANE Select	ENSP00000457473.1:p.Val498Ala
ENST00000574918.2:c.1358T>C	ENSP00000460214.2:p.Val453Ala
ENST00000682050.1:c.*192T>C	ENSP00000508367.1:n.*192T>C
ENST00000219833.12:c.1493T>C	ENSP00000219833.8:p.Val498Ala
ENST00000379906.6:c.1493T>C	ENSP00000369237.2:p.Val498Ala
ENST00000414754.7:c.1493T>C	ENSP00000394956.3:p.Val498Ala
ENST00000561820.5:c.1493T>C	ENSP00000454439.1:p.Val498Ala
ENST00000566163.5:c.1358T>C	ENSP00000456210.1:p.Val453Ala
ENST00000567238.1:c.1178T>C	ENSP00000457375.1:p.Val393Ala
ENST00000568943.5:c.1493T>C	ENSP00000457473.1:p.Val498Ala
NM_001043.3:c.1493T>C	NP_001034.1:p.Val498Ala
NM_001172501.1:c.1493T>C	NP_001165972.1:p.Val498Ala
NM_001172502.1:c.1178T>C	NP_001165973.1:p.Val393Ala
NM_001172504.1:c.1493T>C	NP_001165975.1:p.Val498Ala
XM_006721263.2:c.1493T>C	XP_006721326.1:p.Val498Ala
XM_011523295.1:c.1493T>C	XP_011521597.1:p.Val498Ala
XM_011523296.1:c.1358T>C	XP_011521598.1:p.Val453Ala
XM_011523297.1:c.1358T>C	XP_011521599.1:p.Val453Ala
XM_011523299.1:c.770T>C	XP_011521601.1:p.Val257Ala
XM_011523300.1:c.770T>C	XP_011521602.1:p.Val257Ala
XR_933403.1:n.2107-582T>C
XM_011523295.2:c.1493T>C	XP_011521597.1:p.Val498Ala
XM_011523296.2:c.1358T>C	XP_011521598.1:p.Val453Ala
XM_011523297.3:c.1358T>C	XP_011521599.1:p.Val453Ala
XM_011523299.2:c.770T>C	XP_011521601.1:p.Val257Ala
XM_011523300.2:c.770T>C	XP_011521602.1:p.Val257Ala
XR_933403.3:n.1783-582T>C
NM_001172501.2:c.1493T>C	NP_001165972.1:p.Val498Ala
NM_001172501.3:c.1493T>C MANE Select	NP_001165972.1:p.Val498Ala