Canonical Allele Identifier: CA2466438086
Gene: SLC6A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153693908C= , CM000685.2:g.153693908C= GRCh38
NC_000023.10:g.152959363C= , CM000685.1:g.152959363C= GRCh37
NC_000023.9:g.152612557C= NCBI36
NG_012016.1:g.10612C=
NG_012016.2:g.10612C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.1145C= MANE Select ENSP00000253122.5:p.Pro382=
ENST00000253122.9:c.1145C= ENSP00000253122.5:p.Pro382=
ENST00000413787.1:c.258-296C= ENSP00000400463.1:n.258-296C=
ENST00000430077.6:c.800C= ENSP00000403041.2:p.Pro267=
ENST00000442457.1:c.199C=
ENST00000457723.1:c.129C= ENSP00000394742.1:p.Ala43=
ENST00000467402.1:n.244C=
ENST00000485324.1:n.1178C=
NM_001142805.1:c.1115C= NP_001136277.1:p.Pro372=
NM_001142806.1:c.800C= NP_001136278.1:p.Pro267=
NM_005629.3:c.1145C= NP_005620.1:p.Pro382=
NM_005629.4:c.1145C= MANE Select NP_005620.1:p.Pro382=
NM_001142805.2:c.1115C= NP_001136277.1:p.Pro372=