Canonical Allele Identifier: CA2575996805
Gene: SLC6A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55699708A>G , CM000678.2:g.55699708A>G GRCh38
NC_000016.9:g.55733620A>G , CM000678.1:g.55733620A>G GRCh37
NC_000016.8:g.54291121A>G NCBI36
NG_016969.1:g.49079A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000219833.13:c.1590+54A>G ENSP00000219833.8:n.1590+54A>G
ENST00000568943.6:c.1590+54A>G MANE Select ENSP00000457473.1:n.1590+54A>G
ENST00000574918.2:c.1455+54A>G ENSP00000460214.2:n.1455+54A>G
ENST00000682050.1:c.*289+54A>G ENSP00000508367.1:n.*289+54A>G
ENST00000219833.12:c.1590+54A>G ENSP00000219833.8:n.1590+54A>G
ENST00000379906.6:c.1590+54A>G ENSP00000369237.2:n.1590+54A>G
ENST00000414754.7:c.1590+54A>G ENSP00000394956.3:n.1590+54A>G
ENST00000561820.5:c.1590+54A>G ENSP00000454439.1:n.1590+54A>G
ENST00000566163.5:c.1455+54A>G ENSP00000456210.1:n.1455+54A>G
ENST00000567238.1:c.1275+54A>G ENSP00000457375.1:n.1275+54A>G
ENST00000568943.5:c.1590+54A>G ENSP00000457473.1:n.1590+54A>G
NM_001043.3:c.1590+54A>G NP_001034.1:n.1590+54A>G
NM_001172501.1:c.1590+54A>G NP_001165972.1:n.1590+54A>G
NM_001172502.1:c.1275+54A>G NP_001165973.1:n.1275+54A>G
NM_001172504.1:c.1590+54A>G NP_001165975.1:n.1590+54A>G
XM_006721263.2:c.1590+54A>G XP_006721326.1:n.1590+54A>G
XM_011523295.1:c.1590+54A>G XP_011521597.1:n.1590+54A>G
XM_011523296.1:c.1455+54A>G XP_011521598.1:n.1455+54A>G
XM_011523297.1:c.1455+54A>G XP_011521599.1:n.1455+54A>G
XM_011523299.1:c.867+54A>G XP_011521601.1:n.867+54A>G
XM_011523300.1:c.867+54A>G XP_011521602.1:n.867+54A>G
XR_933403.1:n.2107-431A>G
XM_011523295.2:c.1590+54A>G XP_011521597.1:n.1590+54A>G
XM_011523296.2:c.1455+54A>G XP_011521598.1:n.1455+54A>G
XM_011523297.3:c.1455+54A>G XP_011521599.1:n.1455+54A>G
XM_011523299.2:c.867+54A>G XP_011521601.1:n.867+54A>G
XM_011523300.2:c.867+54A>G XP_011521602.1:n.867+54A>G
XR_933403.3:n.1783-431A>G
NM_001172501.2:c.1590+54A>G NP_001165972.1:n.1590+54A>G
NM_001172501.3:c.1590+54A>G MANE Select NP_001165972.1:n.1590+54A>G