Canonical Allele Identifier: CA2370267416

Gene: CYP24A1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54164329_54164331delinsCTG , CM000682.2:g.54164329_54164331delinsCTG	GRCh38
NC_000020.10:g.52780868_52780870delinsCTG , CM000682.1:g.52780868_52780870delinsCTG	GRCh37
NC_000020.9:g.52214275_52214277delinsCTG	NCBI36
NG_008334.1:g.14647_14649delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216862.8:c.844+121_844+123delinsCAG MANE Select	ENSP00000216862.3:n.844+121_844+123delinsCAG
ENST00000216862.7:c.844+121_844+123delinsCAG	ENSP00000216862.3:n.844+121_844+123delinsCAG
ENST00000395954.3:c.418+121_418+123delinsCAG	ENSP00000379284.3:n.418+121_418+123delinsCAG
ENST00000395955.7:c.844+121_844+123delinsCAG	ENSP00000379285.3:n.844+121_844+123delinsCAG
ENST00000487593.1:n.97+121_97+123delinsCAG
NM_000782.4:c.844+121_844+123delinsCAG	NP_000773.2:n.844+121_844+123delinsCAG
NM_001128915.1:c.844+121_844+123delinsCAG	NP_001122387.1:n.844+121_844+123delinsCAG
XM_005260304.3:c.844+121_844+123delinsCAG	XP_005260361.1:n.844+121_844+123delinsCAG
XM_005260304.5:c.844+121_844+123delinsCAG	XP_005260361.1:n.844+121_844+123delinsCAG
XM_017027691.2:c.844+121_844+123delinsCAG	XP_016883180.1:n.844+121_844+123delinsCAG
XM_017027692.2:c.844+121_844+123delinsCAG	XP_016883181.1:n.844+121_844+123delinsCAG
XM_017027693.2:c.844+121_844+123delinsCAG	XP_016883182.1:n.844+121_844+123delinsCAG
NM_000782.5:c.844+121_844+123delinsCAG MANE Select	NP_000773.2:n.844+121_844+123delinsCAG
NM_001128915.2:c.844+121_844+123delinsCAG	NP_001122387.1:n.844+121_844+123delinsCAG