Canonical Allele Identifier: CA415086489
Gene: SLC6A8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153693974C>A , CM000685.2:g.153693974C>A GRCh38
NC_000023.10:g.152959429C>A , CM000685.1:g.152959429C>A GRCh37
NC_000023.9:g.152612623C>A NCBI36
NG_012016.1:g.10678C>A
NG_012016.2:g.10678C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.1211C>A MANE Select ENSP00000253122.5:p.Ala404Asp
ENST00000253122.9:c.1211C>A ENSP00000253122.5:p.Ala404Asp
ENST00000413787.1:c.258-230C>A ENSP00000400463.1:n.258-230C>A
ENST00000430077.6:c.866C>A ENSP00000403041.2:p.Ala289Asp
ENST00000442457.1:c.265C>A
ENST00000457723.1:c.195C>A ENSP00000394742.1:p.Cys65Ter
ENST00000485324.1:n.1244C>A
NM_001142805.1:c.1181C>A NP_001136277.1:p.Ala394Asp
NM_001142806.1:c.866C>A NP_001136278.1:p.Ala289Asp
NM_005629.3:c.1211C>A NP_005620.1:p.Ala404Asp
NM_005629.4:c.1211C>A MANE Select NP_005620.1:p.Ala404Asp
NM_001142805.2:c.1181C>A NP_001136277.1:p.Ala394Asp