Canonical Allele Identifier: CA2807127270
Gene: SLC6A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55696396_55696397insCAAACACACCC , CM000678.2:g.55696396_55696397insCAAACACACCC GRCh38
NC_000016.9:g.55730308_55730309insCAAACACACCC , CM000678.1:g.55730308_55730309insCAAACACACCC GRCh37
NC_000016.8:g.54287809_54287810insCAAACACACCC NCBI36
NG_016969.1:g.45767_45768insCAAACACACCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000219833.13:c.1260+59_1260+60insCAAACACACCC ENSP00000219833.8:n.1260+59_1260+60insCAAACACACCC
ENST00000568943.6:c.1260+59_1260+60insCAAACACACCC MANE Select ENSP00000457473.1:n.1260+59_1260+60insCAAACACACCC
ENST00000574918.2:c.1125+59_1125+60insCAAACACACCC ENSP00000460214.2:n.1125+59_1125+60insCAAACACACCC
ENST00000682050.1:c.1012+994_1012+995insCAAACACACCC ENSP00000508367.1:n.1012+994_1012+995insCAAACACACCC
ENST00000219833.12:c.1260+59_1260+60insCAAACACACCC ENSP00000219833.8:n.1260+59_1260+60insCAAACACACCC
ENST00000379906.6:c.1260+59_1260+60insCAAACACACCC ENSP00000369237.2:n.1260+59_1260+60insCAAACACACCC
ENST00000414754.7:c.1260+59_1260+60insCAAACACACCC ENSP00000394956.3:n.1260+59_1260+60insCAAACACACCC
ENST00000561820.5:c.1260+59_1260+60insCAAACACACCC ENSP00000454439.1:n.1260+59_1260+60insCAAACACACCC
ENST00000566163.5:c.1125+59_1125+60insCAAACACACCC ENSP00000456210.1:n.1125+59_1125+60insCAAACACACCC
ENST00000567238.1:c.945+59_945+60insCAAACACACCC ENSP00000457375.1:n.945+59_945+60insCAAACACACCC
ENST00000568943.5:c.1260+59_1260+60insCAAACACACCC ENSP00000457473.1:n.1260+59_1260+60insCAAACACACCC
NM_001043.3:c.1260+59_1260+60insCAAACACACCC NP_001034.1:n.1260+59_1260+60insCAAACACACCC
NM_001172501.1:c.1260+59_1260+60insCAAACACACCC NP_001165972.1:n.1260+59_1260+60insCAAACACACCC
NM_001172502.1:c.945+59_945+60insCAAACACACCC NP_001165973.1:n.945+59_945+60insCAAACACACCC
NM_001172504.1:c.1260+59_1260+60insCAAACACACCC NP_001165975.1:n.1260+59_1260+60insCAAACACACCC
XM_006721263.2:c.1260+59_1260+60insCAAACACACCC XP_006721326.1:n.1260+59_1260+60insCAAACACACCC
XM_011523295.1:c.1260+59_1260+60insCAAACACACCC XP_011521597.1:n.1260+59_1260+60insCAAACACACCC
XM_011523296.1:c.1125+59_1125+60insCAAACACACCC XP_011521598.1:n.1125+59_1125+60insCAAACACACCC
XM_011523297.1:c.1125+59_1125+60insCAAACACACCC XP_011521599.1:n.1125+59_1125+60insCAAACACACCC
XM_011523298.1:c.1147+994_1147+995insCAAACACACCC XP_011521600.1:n.1147+994_1147+995insCAAACACACCC
XM_011523299.1:c.537+59_537+60insCAAACACACCC XP_011521601.1:n.537+59_537+60insCAAACACACCC
XM_011523300.1:c.537+59_537+60insCAAACACACCC XP_011521602.1:n.537+59_537+60insCAAACACACCC
XR_933403.1:n.1877+59_1877+60insCAAACACACCC
XM_011523295.2:c.1260+59_1260+60insCAAACACACCC XP_011521597.1:n.1260+59_1260+60insCAAACACACCC
XM_011523296.2:c.1125+59_1125+60insCAAACACACCC XP_011521598.1:n.1125+59_1125+60insCAAACACACCC
XM_011523297.3:c.1125+59_1125+60insCAAACACACCC XP_011521599.1:n.1125+59_1125+60insCAAACACACCC
XM_011523298.2:c.1147+994_1147+995insCAAACACACCC XP_011521600.1:n.1147+994_1147+995insCAAACACACCC
XM_011523299.2:c.537+59_537+60insCAAACACACCC XP_011521601.1:n.537+59_537+60insCAAACACACCC
XM_011523300.2:c.537+59_537+60insCAAACACACCC XP_011521602.1:n.537+59_537+60insCAAACACACCC
XR_933403.3:n.1553+59_1553+60insCAAACACACCC
NM_001172501.2:c.1260+59_1260+60insCAAACACACCC NP_001165972.1:n.1260+59_1260+60insCAAACACACCC
NM_001172501.3:c.1260+59_1260+60insCAAACACACCC MANE Select NP_001165972.1:n.1260+59_1260+60insCAAACACACCC