Canonical Allele Identifier: CA2370267394

Gene: CYP24A1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54164256_54164258delinsCTT , CM000682.2:g.54164256_54164258delinsCTT	GRCh38
NC_000020.10:g.52780795_52780797delinsCTT , CM000682.1:g.52780795_52780797delinsCTT	GRCh37
NC_000020.9:g.52214202_52214204delinsCTT	NCBI36
NG_008334.1:g.14720_14722delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216862.8:c.844+194_844+196delinsAAG MANE Select	ENSP00000216862.3:n.844+194_844+196delinsAAG
ENST00000216862.7:c.844+194_844+196delinsAAG	ENSP00000216862.3:n.844+194_844+196delinsAAG
ENST00000395954.3:c.418+194_418+196delinsAAG	ENSP00000379284.3:n.418+194_418+196delinsAAG
ENST00000395955.7:c.844+194_844+196delinsAAG	ENSP00000379285.3:n.844+194_844+196delinsAAG
ENST00000487593.1:n.97+194_97+196delinsAAG
NM_000782.4:c.844+194_844+196delinsAAG	NP_000773.2:n.844+194_844+196delinsAAG
NM_001128915.1:c.844+194_844+196delinsAAG	NP_001122387.1:n.844+194_844+196delinsAAG
XM_005260304.3:c.844+194_844+196delinsAAG	XP_005260361.1:n.844+194_844+196delinsAAG
XM_005260304.5:c.844+194_844+196delinsAAG	XP_005260361.1:n.844+194_844+196delinsAAG
XM_017027691.2:c.844+194_844+196delinsAAG	XP_016883180.1:n.844+194_844+196delinsAAG
XM_017027692.2:c.844+194_844+196delinsAAG	XP_016883181.1:n.844+194_844+196delinsAAG
XM_017027693.2:c.844+194_844+196delinsAAG	XP_016883182.1:n.844+194_844+196delinsAAG
NM_000782.5:c.844+194_844+196delinsAAG MANE Select	NP_000773.2:n.844+194_844+196delinsAAG
NM_001128915.2:c.844+194_844+196delinsAAG	NP_001122387.1:n.844+194_844+196delinsAAG