Canonical Allele Identifier: CA2370270070
Community Standard Title: NM_000782.5(CYP24A1):c.552C= (p.Ala184=)
Gene: CYP24A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54169680G= , CM000682.2:g.54169680G= GRCh38
NC_000020.10:g.52786219G= , CM000682.1:g.52786219G= GRCh37
NC_000020.9:g.52219626G= NCBI36
NG_008334.1:g.9298C=

Transcript Alleles

HGVS Amino-acid Change
NM_000782.5:c.552C= MANE Select NP_000773.2:p.Ala184=
ENST00000216862.8:c.552C= MANE Select ENSP00000216862.3:p.Ala184=
NM_000782.4:c.552C= NP_000773.2:p.Ala184=
NM_001128915.1:c.552C= NP_001122387.1:p.Ala184=
NM_001128915.2:c.552C= NP_001122387.1:p.Ala184=
ENST00000216862.7:c.552C= ENSP00000216862.3:p.Ala184=
ENST00000395954.3:c.126C= ENSP00000379284.3:p.Ala42=
ENST00000395955.7:c.552C= ENSP00000379285.3:p.Ala184=
XM_005260304.3:c.552C= XP_005260361.1:p.Ala184=
XM_005260304.5:c.552C= XP_005260361.1:p.Ala184=
XM_017027691.2:c.552C= XP_016883180.1:p.Ala184=
XM_017027692.2:c.552C= XP_016883181.1:p.Ala184=
XM_017027693.2:c.552C= XP_016883182.1:p.Ala184=