Canonical Allele Identifier: CA2466438115
Gene: SLC6A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153693981C= , CM000685.2:g.153693981C= GRCh38
NC_000023.10:g.152959436C= , CM000685.1:g.152959436C= GRCh37
NC_000023.9:g.152612630C= NCBI36
NG_012016.1:g.10685C=
NG_012016.2:g.10685C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.1218C= MANE Select ENSP00000253122.5:p.Phe406=
ENST00000253122.9:c.1218C= ENSP00000253122.5:p.Phe406=
ENST00000413787.1:c.258-223C= ENSP00000400463.1:n.258-223C=
ENST00000430077.6:c.873C= ENSP00000403041.2:p.Phe291=
ENST00000442457.1:c.272C=
ENST00000457723.1:c.202C= ENSP00000394742.1:p.Leu68=
ENST00000485324.1:n.1251C=
NM_001142805.1:c.1188C= NP_001136277.1:p.Phe396=
NM_001142806.1:c.873C= NP_001136278.1:p.Phe291=
NM_005629.3:c.1218C= NP_005620.1:p.Phe406=
NM_005629.4:c.1218C= MANE Select NP_005620.1:p.Phe406=
NM_001142805.2:c.1188C= NP_001136277.1:p.Phe396=