Canonical Allele Identifier: CA745612269

Gene: CYP24A1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54156202T>A , CM000682.2:g.54156202T>A	GRCh38
NC_000020.10:g.52772741T>A , CM000682.1:g.52772741T>A	GRCh37
NC_000020.9:g.52206148T>A	NCBI36
NG_008334.1:g.22776A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216862.8:c.*10+967A>T MANE Select	ENSP00000216862.3:n.*10+967A>T
ENST00000216862.7:c.*10+967A>T	ENSP00000216862.3:n.*10+967A>T
ENST00000395954.3:c.*10+967A>T	ENSP00000379284.3:n.*10+967A>T
ENST00000395955.7:c.*10+967A>T	ENSP00000379285.3:n.*10+967A>T
ENST00000460643.1:n.130+967A>T
NM_000782.4:c.*10+967A>T	NP_000773.2:n.*10+967A>T
NM_001128915.1:c.*10+967A>T	NP_001122387.1:n.*10+967A>T
XM_005260304.3:c.*10+967A>T	XP_005260361.1:n.*10+967A>T
XM_005260304.5:c.*10+967A>T	XP_005260361.1:n.*10+967A>T
XM_017027691.2:c.*10+967A>T	XP_016883180.1:n.*10+967A>T
XM_017027692.2:c.*10+967A>T	XP_016883181.1:n.*10+967A>T
XM_017027693.2:c.*10+967A>T	XP_016883182.1:n.*10+967A>T
NM_000782.5:c.*10+967A>T MANE Select	NP_000773.2:n.*10+967A>T
NM_001128915.2:c.*10+967A>T	NP_001122387.1:n.*10+967A>T