Canonical Allele Identifier: CA281442535

Gene: SLC6A2

Linked Data

• dbSNP Id: rs34828426
• MyVariant Identifiers: chr16:g.55702607del (hg19) ; chr16:g.55668695del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55668696del , CM000678.2:g.55668696del	GRCh38
NC_000016.9:g.55702608del , CM000678.1:g.55702608del	GRCh37
NC_000016.8:g.54260109del	NCBI36
NG_016969.1:g.18067del

Transcript Alleles

HGVS	Amino-acid change
ENST00000219833.13:c.275-869del	ENSP00000219833.8:n.275-869del
ENST00000568943.6:c.275-869del MANE Select	ENSP00000457473.1:n.275-869del
ENST00000574918.2:c.275-869del	ENSP00000460214.2:n.275-869del
ENST00000682050.1:c.275-869del	ENSP00000508367.1:n.275-869del
ENST00000219833.12:c.275-869del	ENSP00000219833.8:n.275-869del
ENST00000379906.6:c.275-869del	ENSP00000369237.2:n.275-869del
ENST00000414754.7:c.275-869del	ENSP00000394956.3:n.275-869del
ENST00000561820.5:c.275-869del	ENSP00000454439.1:n.275-869del
ENST00000566163.5:c.275-869del	ENSP00000456210.1:n.275-869del
ENST00000568529.6:c.275-869del	ENSP00000456377.2:n.275-869del
ENST00000568655.5:c.275-869del	ENSP00000454603.1:n.275-869del
ENST00000568943.5:c.275-869del	ENSP00000457473.1:n.275-869del
NM_001043.3:c.275-869del	NP_001034.1:n.275-869del
NM_001172501.1:c.275-869del	NP_001165972.1:n.275-869del
NM_001172504.1:c.275-869del	NP_001165975.1:n.275-869del
XM_006721263.2:c.275-869del	XP_006721326.1:n.275-869del
XM_011523295.1:c.275-869del	XP_011521597.1:n.275-869del
XM_011523296.1:c.275-869del	XP_011521598.1:n.275-869del
XM_011523297.1:c.275-869del	XP_011521599.1:n.275-869del
XM_011523298.1:c.275-869del	XP_011521600.1:n.275-869del
XR_933403.1:n.892-869del
XM_011523295.2:c.275-869del	XP_011521597.1:n.275-869del
XM_011523296.2:c.275-869del	XP_011521598.1:n.275-869del
XM_011523297.3:c.275-869del	XP_011521599.1:n.275-869del
XM_011523298.2:c.275-869del	XP_011521600.1:n.275-869del
XR_933403.3:n.568-869del
NM_001172501.2:c.275-869del	NP_001165972.1:n.275-869del
NM_001172501.3:c.275-869del MANE Select	NP_001165972.1:n.275-869del