Canonical Allele Identifier: CA2370272020

Gene: CYP24A1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54173686_54173688delinsCAA , CM000682.2:g.54173686_54173688delinsCAA	GRCh38
NC_000020.10:g.52790225_52790227delinsCAA , CM000682.1:g.52790225_52790227delinsCAA	GRCh37
NC_000020.9:g.52223632_52223634delinsCAA	NCBI36
NG_008334.1:g.5290_5292delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216862.8:c.-109_-107delinsTTG MANE Select	ENSP00000216862.3:n.-109_-107delinsTTG
ENST00000216862.7:c.-109_-107delinsTTG	ENSP00000216862.3:n.-109_-107delinsTTG
NM_000782.4:c.-109_-107delinsTTG	NP_000773.2:n.-109_-107delinsTTG
NM_001128915.1:c.-109_-107delinsTTG	NP_001122387.1:n.-109_-107delinsTTG
XM_005260304.3:c.-109_-107delinsTTG	XP_005260361.1:n.-109_-107delinsTTG
XM_005260304.5:c.-109_-107delinsTTG	XP_005260361.1:n.-109_-107delinsTTG
XM_017027691.2:c.-109_-107delinsTTG	XP_016883180.1:n.-109_-107delinsTTG
XM_017027692.2:c.-109_-107delinsTTG	XP_016883181.1:n.-109_-107delinsTTG
XM_017027693.2:c.-109_-107delinsTTG	XP_016883182.1:n.-109_-107delinsTTG
NM_000782.5:c.-109_-107delinsTTG MANE Select	NP_000773.2:n.-109_-107delinsTTG
NM_001128915.2:c.-109_-107delinsTTG	NP_001122387.1:n.-109_-107delinsTTG