Canonical Allele Identifier: CA2807126297

Gene: SLC6A2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55656155del , CM000678.2:g.55656155del	GRCh38
NC_000016.9:g.55690067del , CM000678.1:g.55690067del	GRCh37
NC_000016.8:g.54247568del	NCBI36
NG_016969.1:g.5526del

Transcript Alleles

HGVS	Amino-acid change
ENST00000568943.6:c.-66del MANE Select	ENSP00000457473.1:n.-66del
ENST00000414754.7:c.-66del	ENSP00000394956.3:n.-66del
ENST00000568529.6:c.-66del	ENSP00000456377.2:n.-66del
ENST00000568943.5:c.-66del	ENSP00000457473.1:n.-66del
NM_001172501.1:c.-66del	NP_001165972.1:n.-66del
XM_011523295.1:c.-66del	XP_011521597.1:n.-66del
XM_011523296.1:c.-66del	XP_011521598.1:n.-66del
XM_011523297.1:c.-66del	XP_011521599.1:n.-66del
XM_011523298.1:c.-66del	XP_011521600.1:n.-66del
XR_933403.1:n.552del
XM_011523295.2:c.-66del	XP_011521597.1:n.-66del
XM_011523296.2:c.-66del	XP_011521598.1:n.-66del
XM_011523297.3:c.-66del	XP_011521599.1:n.-66del
XM_011523298.2:c.-66del	XP_011521600.1:n.-66del
XR_933403.3:n.228del
NM_001172501.2:c.-66del	NP_001165972.1:n.-66del
NM_001172501.3:c.-66del MANE Select	NP_001165972.1:n.-66del