Canonical Allele Identifier: CA2633287326

Gene: SLC6A2

Linked Data

• gnomAD v4: 16-55656134-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55656135del , CM000678.2:g.55656135del	GRCh38
NC_000016.9:g.55690047del , CM000678.1:g.55690047del	GRCh37
NC_000016.8:g.54247548del	NCBI36
NG_016969.1:g.5506del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568943.6:c.-86del MANE Select	ENSP00000457473.1:n.-86del
ENST00000414754.7:c.-86del	ENSP00000394956.3:n.-86del
ENST00000568529.6:c.-86del	ENSP00000456377.2:n.-86del
ENST00000568943.5:c.-86del	ENSP00000457473.1:n.-86del
NM_001172501.1:c.-86del	NP_001165972.1:n.-86del
XM_011523295.1:c.-86del	XP_011521597.1:n.-86del
XM_011523296.1:c.-86del	XP_011521598.1:n.-86del
XM_011523297.1:c.-86del	XP_011521599.1:n.-86del
XM_011523298.1:c.-86del	XP_011521600.1:n.-86del
XR_933403.1:n.532del
XM_011523295.2:c.-86del	XP_011521597.1:n.-86del
XM_011523296.2:c.-86del	XP_011521598.1:n.-86del
XM_011523297.3:c.-86del	XP_011521599.1:n.-86del
XM_011523298.2:c.-86del	XP_011521600.1:n.-86del
XR_933403.3:n.208del
NM_001172501.2:c.-86del	NP_001165972.1:n.-86del
NM_001172501.3:c.-86del MANE Select	NP_001165972.1:n.-86del