Canonical Allele Identifier: CA2466438214
Gene: SLC6A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153694175C= , CM000685.2:g.153694175C= GRCh38
NC_000023.10:g.152959630C= , CM000685.1:g.152959630C= GRCh37
NC_000023.9:g.152612824C= NCBI36
NG_012016.1:g.10879C=
NG_012016.2:g.10879C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.1300C= MANE Select ENSP00000253122.5:p.Pro434=
ENST00000253122.9:c.1300C= ENSP00000253122.5:p.Pro434=
ENST00000413787.1:c.258-29C= ENSP00000400463.1:n.258-29C=
ENST00000430077.6:c.955C= ENSP00000403041.2:p.Pro319=
ENST00000442457.1:c.354C=
ENST00000485324.1:n.1445C=
NM_001142805.1:c.1270C= NP_001136277.1:p.Pro424=
NM_001142806.1:c.955C= NP_001136278.1:p.Pro319=
NM_005629.3:c.1300C= NP_005620.1:p.Pro434=
NM_005629.4:c.1300C= MANE Select NP_005620.1:p.Pro434=
NM_001142805.2:c.1270C= NP_001136277.1:p.Pro424=