Canonical Allele Identifier: CA2837944772

Gene: CYP24A1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54173718_54173726dup , CM000682.2:g.54173718_54173726dup	GRCh38
NC_000020.10:g.52790257_52790265dup , CM000682.1:g.52790257_52790265dup	GRCh37
NC_000020.9:g.52223664_52223672dup	NCBI36
NG_008334.1:g.5255_5263dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216862.8:c.-144_-136dup MANE Select	ENSP00000216862.3:n.-144_-136dup
ENST00000216862.7:c.-144_-136dup	ENSP00000216862.3:n.-144_-136dup
NM_000782.4:c.-144_-136dup	NP_000773.2:n.-144_-136dup
NM_001128915.1:c.-144_-136dup	NP_001122387.1:n.-144_-136dup
XM_005260304.3:c.-144_-136dup	XP_005260361.1:n.-144_-136dup
XM_005260304.5:c.-144_-136dup	XP_005260361.1:n.-144_-136dup
XM_017027691.2:c.-144_-136dup	XP_016883180.1:n.-144_-136dup
XM_017027692.2:c.-144_-136dup	XP_016883181.1:n.-144_-136dup
XM_017027693.2:c.-144_-136dup	XP_016883182.1:n.-144_-136dup
NM_000782.5:c.-144_-136dup MANE Select	NP_000773.2:n.-144_-136dup
NM_001128915.2:c.-144_-136dup	NP_001122387.1:n.-144_-136dup