Canonical Allele Identifier: CA2466438113
Gene: SLC6A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153693977T= , CM000685.2:g.153693977T= GRCh38
NC_000023.10:g.152959432T= , CM000685.1:g.152959432T= GRCh37
NC_000023.9:g.152612626T= NCBI36
NG_012016.1:g.10681T=
NG_012016.2:g.10681T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.1214T= MANE Select ENSP00000253122.5:p.Leu405=
ENST00000253122.9:c.1214T= ENSP00000253122.5:p.Leu405=
ENST00000413787.1:c.258-227T= ENSP00000400463.1:n.258-227T=
ENST00000430077.6:c.869T= ENSP00000403041.2:p.Leu290=
ENST00000442457.1:c.268T=
ENST00000457723.1:c.198T= ENSP00000394742.1:p.Pro66=
ENST00000485324.1:n.1247T=
NM_001142805.1:c.1184T= NP_001136277.1:p.Leu395=
NM_001142806.1:c.869T= NP_001136278.1:p.Leu290=
NM_005629.3:c.1214T= NP_005620.1:p.Leu405=
NM_005629.4:c.1214T= MANE Select NP_005620.1:p.Leu405=
NM_001142805.2:c.1184T= NP_001136277.1:p.Leu395=