Canonical Allele Identifier: CA415086922
Gene: SLC6A8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153694218C>T , CM000685.2:g.153694218C>T GRCh38
NC_000023.10:g.152959673C>T , CM000685.1:g.152959673C>T GRCh37
NC_000023.9:g.152612867C>T NCBI36
NG_012016.1:g.10922C>T
NG_012016.2:g.10922C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.1343C>T MANE Select ENSP00000253122.5:p.Ala448Val
ENST00000253122.9:c.1343C>T ENSP00000253122.5:p.Ala448Val
ENST00000413787.1:c.272C>T ENSP00000400463.1:p.Ala91Val
ENST00000430077.6:c.998C>T ENSP00000403041.2:p.Ala333Val
ENST00000442457.1:c.397C>T
ENST00000485324.1:n.1488C>T
NM_001142805.1:c.1313C>T NP_001136277.1:p.Ala438Val
NM_001142806.1:c.998C>T NP_001136278.1:p.Ala333Val
NM_005629.3:c.1343C>T NP_005620.1:p.Ala448Val
NM_005629.4:c.1343C>T MANE Select NP_005620.1:p.Ala448Val
NM_001142805.2:c.1313C>T NP_001136277.1:p.Ala438Val