Canonical Allele Identifier: CA2999953081

Gene: SLC6A2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55656455del , CM000678.2:g.55656455del	GRCh38
NC_000016.9:g.55690367del , CM000678.1:g.55690367del	GRCh37
NC_000016.8:g.54247868del	NCBI36
NG_016969.1:g.5826del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219833.13:c.-240del	ENSP00000219833.8:n.-240del
ENST00000568943.6:c.-51-189del MANE Select	ENSP00000457473.1:n.-51-189del
ENST00000574918.2:c.-52+103del	ENSP00000460214.2:n.-52+103del
ENST00000682050.1:c.-52+103del	ENSP00000508367.1:n.-52+103del
ENST00000379906.6:c.-240del	ENSP00000369237.2:n.-240del
ENST00000414754.7:c.-51-189del	ENSP00000394956.3:n.-51-189del
ENST00000568529.6:c.-51-189del	ENSP00000456377.2:n.-51-189del
ENST00000568655.5:c.-52+103del	ENSP00000454603.1:n.-52+103del
ENST00000568943.5:c.-51-189del	ENSP00000457473.1:n.-51-189del
NM_001043.3:c.-240del	NP_001034.1:n.-240del
NM_001172501.1:c.-51-189del	NP_001165972.1:n.-51-189del
XM_006721263.2:c.-52+103del	XP_006721326.1:n.-52+103del
XM_011523295.1:c.-51-189del	XP_011521597.1:n.-51-189del
XM_011523296.1:c.-51-189del	XP_011521598.1:n.-51-189del
XM_011523297.1:c.-51-189del	XP_011521599.1:n.-51-189del
XM_011523298.1:c.-51-189del	XP_011521600.1:n.-51-189del
XR_933403.1:n.567-189del
XM_011523295.2:c.-51-189del	XP_011521597.1:n.-51-189del
XM_011523296.2:c.-51-189del	XP_011521598.1:n.-51-189del
XM_011523297.3:c.-51-189del	XP_011521599.1:n.-51-189del
XM_011523298.2:c.-51-189del	XP_011521600.1:n.-51-189del
XR_933403.3:n.243-189del
NM_001172501.2:c.-51-189del	NP_001165972.1:n.-51-189del
NM_001172501.3:c.-51-189del MANE Select	NP_001165972.1:n.-51-189del