Canonical Allele Identifier: CA130777
Gene: CYP24A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 29681
ClinVar RCV Id: RCV003556068
dbSNP Id: rs387907324

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54162743C>T , CM000682.2:g.54162743C>T GRCh38
NC_000020.10:g.52779282C>T , CM000682.1:g.52779282C>T GRCh37
NC_000020.9:g.52212689C>T NCBI36
NG_008334.1:g.16235G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000216862.8:c.964G>A MANE Select ENSP00000216862.3:p.Glu322Lys
ENST00000216862.7:c.964G>A ENSP00000216862.3:p.Glu322Lys
ENST00000395954.3:c.538G>A ENSP00000379284.3:p.Glu180Lys
ENST00000395955.7:c.964G>A ENSP00000379285.3:p.Glu322Lys
ENST00000487593.1:n.217G>A
NM_000782.4:c.964G>A NP_000773.2:p.Glu322Lys
NM_001128915.1:c.964G>A NP_001122387.1:p.Glu322Lys
XM_005260304.3:c.964G>A XP_005260361.1:p.Glu322Lys
XM_005260304.5:c.964G>A XP_005260361.1:p.Glu322Lys
XM_017027691.2:c.964G>A XP_016883180.1:p.Glu322Lys
XM_017027692.2:c.964G>A XP_016883181.1:p.Glu322Lys
XM_017027693.2:c.964G>A XP_016883182.1:p.Glu322Lys
NM_000782.5:c.964G>A MANE Select NP_000773.2:p.Glu322Lys
NM_001128915.2:c.964G>A NP_001122387.1:p.Glu322Lys