Canonical Allele Identifier: CA409392101

Gene: CYP24A1

Linked Data

• MyVariant Identifiers: chr20:g.52781103C>A (hg19) ; chr20:g.54164564C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54164564C>A , CM000682.2:g.54164564C>A	GRCh38
NC_000020.10:g.52781103C>A , CM000682.1:g.52781103C>A	GRCh37
NC_000020.9:g.52214510C>A	NCBI36
NG_008334.1:g.14414G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216862.8:c.733-1G>T MANE Select	ENSP00000216862.3:n.733-1G>T
ENST00000216862.7:c.733-1G>T	ENSP00000216862.3:n.733-1G>T
ENST00000395954.3:c.307-1G>T	ENSP00000379284.3:n.307-1G>T
ENST00000395955.7:c.733-1G>T	ENSP00000379285.3:n.733-1G>T
NM_000782.4:c.733-1G>T	NP_000773.2:n.733-1G>T
NM_001128915.1:c.733-1G>T	NP_001122387.1:n.733-1G>T
XM_005260304.3:c.733-1G>T	XP_005260361.1:n.733-1G>T
XM_005260304.5:c.733-1G>T	XP_005260361.1:n.733-1G>T
XM_017027691.2:c.733-1G>T	XP_016883180.1:n.733-1G>T
XM_017027692.2:c.733-1G>T	XP_016883181.1:n.733-1G>T
XM_017027693.2:c.733-1G>T	XP_016883182.1:n.733-1G>T
NM_000782.5:c.733-1G>T MANE Select	NP_000773.2:n.733-1G>T
NM_001128915.2:c.733-1G>T	NP_001122387.1:n.733-1G>T