Canonical Allele Identifier: CA2370272080

Gene: CYP24A1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54173784_54173786delinsCAG , CM000682.2:g.54173784_54173786delinsCAG	GRCh38
NC_000020.10:g.52790323_52790325delinsCAG , CM000682.1:g.52790323_52790325delinsCAG	GRCh37
NC_000020.9:g.52223730_52223732delinsCAG	NCBI36
NG_008334.1:g.5192_5194delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216862.8:c.-207_-205delinsCTG MANE Select	ENSP00000216862.3:n.-207_-205delinsCTG
ENST00000216862.7:c.-207_-205delinsCTG	ENSP00000216862.3:n.-207_-205delinsCTG
NM_000782.4:c.-207_-205delinsCTG	NP_000773.2:n.-207_-205delinsCTG
NM_001128915.1:c.-207_-205delinsCTG	NP_001122387.1:n.-207_-205delinsCTG
XM_005260304.3:c.-207_-205delinsCTG	XP_005260361.1:n.-207_-205delinsCTG
XM_005260304.5:c.-207_-205delinsCTG	XP_005260361.1:n.-207_-205delinsCTG
XM_017027691.2:c.-207_-205delinsCTG	XP_016883180.1:n.-207_-205delinsCTG
XM_017027692.2:c.-207_-205delinsCTG	XP_016883181.1:n.-207_-205delinsCTG
XM_017027693.2:c.-207_-205delinsCTG	XP_016883182.1:n.-207_-205delinsCTG
NM_000782.5:c.-207_-205delinsCTG MANE Select	NP_000773.2:n.-207_-205delinsCTG
NM_001128915.2:c.-207_-205delinsCTG	NP_001122387.1:n.-207_-205delinsCTG