Canonical Allele Identifier: CA2466438225
Gene: SLC6A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153694193C= , CM000685.2:g.153694193C= GRCh38
NC_000023.10:g.152959648C= , CM000685.1:g.152959648C= GRCh37
NC_000023.9:g.152612842C= NCBI36
NG_012016.1:g.10897C=
NG_012016.2:g.10897C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.1318C= MANE Select ENSP00000253122.5:p.Arg440=
ENST00000253122.9:c.1318C= ENSP00000253122.5:p.Arg440=
ENST00000413787.1:c.258-11C= ENSP00000400463.1:n.258-11C=
ENST00000430077.6:c.973C= ENSP00000403041.2:p.Arg325=
ENST00000442457.1:c.372C=
ENST00000485324.1:n.1463C=
NM_001142805.1:c.1288C= NP_001136277.1:p.Arg430=
NM_001142806.1:c.973C= NP_001136278.1:p.Arg325=
NM_005629.3:c.1318C= NP_005620.1:p.Arg440=
NM_005629.4:c.1318C= MANE Select NP_005620.1:p.Arg440=
NM_001142805.2:c.1288C= NP_001136277.1:p.Arg430=