Canonical Allele Identifier: CA392449759
Gene: SLC24A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1938012
ClinVar RCV Id: RCV002646138

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48134300C>T , CM000677.2:g.48134300C>T GRCh38
NC_000015.9:g.48426497C>T , CM000677.1:g.48426497C>T GRCh37
NC_000015.8:g.46213789C>T NCBI36
NG_011500.1:g.18329C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000341459.8:c.344C>T MANE Select ENSP00000341550.3:p.Ala115Val
ENST00000341459.7:c.344C>T ENSP00000341550.3:p.Ala115Val
ENST00000449382.2:c.164C>T ENSP00000389966.2:p.Ala55Val
ENST00000463289.1:n.104C>T
NM_205850.2:c.344C>T NP_995322.1:p.Ala115Val
XM_011521458.1:c.344C>T XP_011519760.1:p.Ala115Val
XM_017022079.1:c.5C>T XP_016877568.1:p.Ala2Val
XM_017022080.1:c.5C>T XP_016877569.1:p.Ala2Val
XM_024449901.1:c.5C>T XP_024305669.1:p.Ala2Val
NM_205850.3:c.344C>T MANE Select NP_995322.1:p.Ala115Val