Canonical Allele Identifier: CA2580089518
Gene: SLC24A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1980113
ClinVar RCV Id: RCV002756391

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48134286_48134287delinsTG , CM000677.2:g.48134286_48134287delinsTG GRCh38
NC_000015.9:g.48426483_48426484delinsTG , CM000677.1:g.48426483_48426484delinsTG GRCh37
NC_000015.8:g.46213775_46213776delinsTG NCBI36
NG_011500.1:g.18315_18316delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000341459.8:c.330_331delinsTG MANE Select ENSP00000341550.3:p.Thr111Ala
ENST00000341459.7:c.330_331delinsTG ENSP00000341550.3:p.Thr111Ala
ENST00000449382.2:c.150_151delinsTG ENSP00000389966.2:p.Thr51Ala
ENST00000463289.1:n.90_91delinsTG
NM_205850.2:c.330_331delinsTG NP_995322.1:p.Thr111Ala
XM_011521458.1:c.330_331delinsTG XP_011519760.1:p.Thr111Ala
XM_017022079.1:c.-10_-9delinsTG XP_016877568.1:n.-10_-9delinsTG
XM_017022080.1:c.-10_-9delinsTG XP_016877569.1:n.-10_-9delinsTG
XM_024449901.1:c.-10_-9delinsTG XP_024305669.1:n.-10_-9delinsTG
NM_205850.3:c.330_331delinsTG MANE Select NP_995322.1:p.Thr111Ala