Canonical Allele Identifier: CA510909818

Gene: CYP24A1

Linked Data

• MyVariant Identifiers: chr20:g.52780992T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54164453T>C , CM000682.2:g.54164453T>C	GRCh38
NC_000020.10:g.52780992T>C , CM000682.1:g.52780992T>C	GRCh37
NC_000020.9:g.52214399T>C	NCBI36
NG_008334.1:g.14525A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216862.8:c.843A>G MANE Select	ENSP00000216862.3:p.Ser281=
ENST00000216862.7:c.843A>G	ENSP00000216862.3:p.Ser281=
ENST00000395954.3:c.417A>G	ENSP00000379284.3:p.Ser139=
ENST00000395955.7:c.843A>G	ENSP00000379285.3:p.Ser281=
ENST00000487593.1:n.96A>G
NM_000782.4:c.843A>G	NP_000773.2:p.Ser281=
NM_001128915.1:c.843A>G	NP_001122387.1:p.Ser281=
XM_005260304.3:c.843A>G	XP_005260361.1:p.Ser281=
XM_005260304.5:c.843A>G	XP_005260361.1:p.Ser281=
XM_017027691.2:c.843A>G	XP_016883180.1:p.Ser281=
XM_017027692.2:c.843A>G	XP_016883181.1:p.Ser281=
XM_017027693.2:c.843A>G	XP_016883182.1:p.Ser281=
NM_000782.5:c.843A>G MANE Select	NP_000773.2:p.Ser281=
NM_001128915.2:c.843A>G	NP_001122387.1:p.Ser281=