Canonical Allele Identifier: CA2466436595
Gene: SLC6A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153690404G= , CM000685.2:g.153690404G= GRCh38
NC_000023.10:g.152955859G= , CM000685.1:g.152955859G= GRCh37
NC_000023.9:g.152609053G= NCBI36
NG_012016.1:g.7108G=
NG_012016.2:g.7108G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.292G= MANE Select ENSP00000253122.5:p.Ala98=
ENST00000675713.1:n.46G=
ENST00000253122.9:c.292G= ENSP00000253122.5:p.Ala98=
ENST00000430077.6:c.-54G= ENSP00000403041.2:n.-54G=
ENST00000476466.1:n.144G=
NM_001142805.1:c.292G= NP_001136277.1:p.Ala98=
NM_001142806.1:c.-54G= NP_001136278.1:n.-54G=
NM_005629.3:c.292G= NP_005620.1:p.Ala98=
NM_005629.4:c.292G= MANE Select NP_005620.1:p.Ala98=
NM_001142805.2:c.292G= NP_001136277.1:p.Ala98=