Canonical Allele Identifier: CA2370263754

Gene: CYP24A1

Genomic Alleles

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

Transcript Alleles

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