Canonical Allele Identifier: CA409391874

Gene: CYP24A1

Linked Data

• MyVariant Identifiers: chr20:g.52781001A>C (hg19) ; chr20:g.54164462A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54164462A>C , CM000682.2:g.54164462A>C	GRCh38
NC_000020.10:g.52781001A>C , CM000682.1:g.52781001A>C	GRCh37
NC_000020.9:g.52214408A>C	NCBI36
NG_008334.1:g.14516T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216862.8:c.834T>G MANE Select	ENSP00000216862.3:p.Ile278Met
ENST00000216862.7:c.834T>G	ENSP00000216862.3:p.Ile278Met
ENST00000395954.3:c.408T>G	ENSP00000379284.3:p.Ile136Met
ENST00000395955.7:c.834T>G	ENSP00000379285.3:p.Ile278Met
ENST00000487593.1:n.87T>G
NM_000782.4:c.834T>G	NP_000773.2:p.Ile278Met
NM_001128915.1:c.834T>G	NP_001122387.1:p.Ile278Met
XM_005260304.3:c.834T>G	XP_005260361.1:p.Ile278Met
XM_005260304.5:c.834T>G	XP_005260361.1:p.Ile278Met
XM_017027691.2:c.834T>G	XP_016883180.1:p.Ile278Met
XM_017027692.2:c.834T>G	XP_016883181.1:p.Ile278Met
XM_017027693.2:c.834T>G	XP_016883182.1:p.Ile278Met
NM_000782.5:c.834T>G MANE Select	NP_000773.2:p.Ile278Met
NM_001128915.2:c.834T>G	NP_001122387.1:p.Ile278Met