Canonical Allele Identifier: CA2577429979
Gene: CYP24A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54173664T>A , CM000682.2:g.54173664T>A GRCh38
NC_000020.10:g.52790203T>A , CM000682.1:g.52790203T>A GRCh37
NC_000020.9:g.52223610T>A NCBI36
NG_008334.1:g.5314A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000216862.8:c.-85A>T MANE Select ENSP00000216862.3:n.-85A>T
ENST00000216862.7:c.-85A>T ENSP00000216862.3:n.-85A>T
NM_000782.4:c.-85A>T NP_000773.2:n.-85A>T
NM_001128915.1:c.-85A>T NP_001122387.1:n.-85A>T
XM_005260304.3:c.-85A>T XP_005260361.1:n.-85A>T
XM_005260304.5:c.-85A>T XP_005260361.1:n.-85A>T
XM_017027691.2:c.-85A>T XP_016883180.1:n.-85A>T
XM_017027692.2:c.-85A>T XP_016883181.1:n.-85A>T
XM_017027693.2:c.-85A>T XP_016883182.1:n.-85A>T
NM_000782.5:c.-85A>T MANE Select NP_000773.2:n.-85A>T
NM_001128915.2:c.-85A>T NP_001122387.1:n.-85A>T