Canonical Allele Identifier: CA519184963
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 511340
dbSNP Id: rs1557044183

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153690466C>T , CM000685.2:g.153690466C>T GRCh38
NC_000023.10:g.152955921C>T , CM000685.1:g.152955921C>T GRCh37
NC_000023.9:g.152609115C>T NCBI36
NG_012016.1:g.7170C>T
NG_012016.2:g.7170C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.354C>T MANE Select ENSP00000253122.5:p.Ala118=
ENST00000675713.1:n.108C>T
ENST00000253122.9:c.354C>T ENSP00000253122.5:p.Ala118=
ENST00000430077.6:c.9C>T ENSP00000403041.2:p.Ala3=
ENST00000476466.1:n.206C>T
NM_001142805.1:c.354C>T NP_001136277.1:p.Ala118=
NM_001142806.1:c.9C>T NP_001136278.1:p.Ala3=
NM_005629.3:c.354C>T NP_005620.1:p.Ala118=
NM_005629.4:c.354C>T MANE Select NP_005620.1:p.Ala118=
NM_001142805.2:c.354C>T NP_001136277.1:p.Ala118=