Canonical Allele Identifier: CA2653391153
Gene: CYP24A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54169574_54169582del , CM000682.2:g.54169574_54169582del GRCh38
NC_000020.10:g.52786113_52786121del , CM000682.1:g.52786113_52786121del GRCh37
NC_000020.9:g.52219520_52219528del NCBI36
NG_008334.1:g.9397_9405del

Transcript Alleles

HGVS Amino-acid change
ENST00000216862.8:c.640+11_640+19del MANE Select ENSP00000216862.3:n.640+11_640+19del
ENST00000216862.7:c.640+11_640+19del ENSP00000216862.3:n.640+11_640+19del
ENST00000395954.3:c.214+11_214+19del ENSP00000379284.3:n.214+11_214+19del
ENST00000395955.7:c.640+11_640+19del ENSP00000379285.3:n.640+11_640+19del
NM_000782.4:c.640+11_640+19del NP_000773.2:n.640+11_640+19del
NM_001128915.1:c.640+11_640+19del NP_001122387.1:n.640+11_640+19del
XM_005260304.3:c.640+11_640+19del XP_005260361.1:n.640+11_640+19del
XM_005260304.5:c.640+11_640+19del XP_005260361.1:n.640+11_640+19del
XM_017027691.2:c.640+11_640+19del XP_016883180.1:n.640+11_640+19del
XM_017027692.2:c.640+11_640+19del XP_016883181.1:n.640+11_640+19del
XM_017027693.2:c.640+11_640+19del XP_016883182.1:n.640+11_640+19del
NM_000782.5:c.640+11_640+19del MANE Select NP_000773.2:n.640+11_640+19del
NM_001128915.2:c.640+11_640+19del NP_001122387.1:n.640+11_640+19del