Canonical Allele Identifier: CA115022
Gene: SLC24A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48134287A= , CM000677.2:g.48134287A= GRCh38
NC_000015.9:g.48426484A= , CM000677.1:g.48426484A= GRCh37
NC_000015.8:g.46213776A= NCBI36
NG_011500.1:g.18316A=

Transcript Alleles

HGVS Amino-acid change
ENST00000341459.8:c.331A= MANE Select ENSP00000341550.3:p.Thr111=
ENST00000341459.7:c.331A= ENSP00000341550.3:p.Thr111=
ENST00000449382.2:c.151A= ENSP00000389966.2:p.Thr51=
ENST00000463289.1:n.91A=
NM_205850.2:c.331A= NP_995322.1:p.Thr111=
XM_011521458.1:c.331A= XP_011519760.1:p.Thr111=
XM_017022079.1:c.-9A= XP_016877568.1:n.-9A=
XM_017022080.1:c.-9A= XP_016877569.1:n.-9A=
XM_024449901.1:c.-9A= XP_024305669.1:n.-9A=
NM_205850.3:c.331A= MANE Select NP_995322.1:p.Thr111=