Canonical Allele Identifier: CA123699
Gene: SLC6A2 HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55698005G>C , CM000678.2:g.55698005G>C GRCh38
NC_000016.9:g.55731917G>C , CM000678.1:g.55731917G>C GRCh37
NC_000016.8:g.54289418G>C NCBI36
NG_016969.1:g.47376G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000219833.13:c.1369G>C ENSP00000219833.8:p.Ala457Pro
ENST00000568943.6:c.1369G>C MANE Select ENSP00000457473.1:p.Ala457Pro
ENST00000574918.2:c.1234G>C ENSP00000460214.2:p.Ala412Pro
ENST00000682050.1:c.*68G>C ENSP00000508367.1:n.*68G>C
ENST00000219833.12:c.1369G>C ENSP00000219833.8:p.Ala457Pro
ENST00000379906.6:c.1369G>C ENSP00000369237.2:p.Ala457Pro
ENST00000414754.7:c.1369G>C ENSP00000394956.3:p.Ala457Pro
ENST00000561820.5:c.1369G>C ENSP00000454439.1:p.Ala457Pro
ENST00000566163.5:c.1234G>C ENSP00000456210.1:p.Ala412Pro
ENST00000567238.1:c.1054G>C ENSP00000457375.1:p.Ala352Pro
ENST00000568943.5:c.1369G>C ENSP00000457473.1:p.Ala457Pro
NM_001043.3:c.1369G>C NP_001034.1:p.Ala457Pro
NM_001172501.1:c.1369G>C NP_001165972.1:p.Ala457Pro
NM_001172502.1:c.1054G>C NP_001165973.1:p.Ala352Pro
NM_001172504.1:c.1369G>C NP_001165975.1:p.Ala457Pro
XM_006721263.2:c.1369G>C XP_006721326.1:p.Ala457Pro
XM_011523295.1:c.1369G>C XP_011521597.1:p.Ala457Pro
XM_011523296.1:c.1234G>C XP_011521598.1:p.Ala412Pro
XM_011523297.1:c.1234G>C XP_011521599.1:p.Ala412Pro
XM_011523298.1:c.*68G>C XP_011521600.1:n.*68G>C
XM_011523299.1:c.646G>C XP_011521601.1:p.Ala216Pro
XM_011523300.1:c.646G>C XP_011521602.1:p.Ala216Pro
XR_933403.1:n.1986G>C
XM_011523295.2:c.1369G>C XP_011521597.1:p.Ala457Pro
XM_011523296.2:c.1234G>C XP_011521598.1:p.Ala412Pro
XM_011523297.3:c.1234G>C XP_011521599.1:p.Ala412Pro
XM_011523298.2:c.*68G>C XP_011521600.1:n.*68G>C
XM_011523299.2:c.646G>C XP_011521601.1:p.Ala216Pro
XM_011523300.2:c.646G>C XP_011521602.1:p.Ala216Pro
XR_933403.3:n.1662G>C
NM_001172501.2:c.1369G>C NP_001165972.1:p.Ala457Pro
NM_001172501.3:c.1369G>C MANE Select NP_001165972.1:p.Ala457Pro