Canonical Allele Identifier: CA2038990906
Gene: CYP27B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57766130_57766131delinsAC , CM000674.2:g.57766130_57766131delinsAC GRCh38
NC_000012.11:g.58159913_58159914delinsAC , CM000674.1:g.58159913_58159914delinsAC GRCh37
NC_000012.10:g.56446180_56446181delinsAC NCBI36
NG_007076.1:g.6063_6064delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000546609.2:n.174_175delinsGT
ENST00000713544.1:c.262_263delinsGT ENSP00000518840.1:p.Val88=
ENST00000713545.1:c.262_263delinsGT ENSP00000518841.1:p.Val88=
ENST00000228606.9:c.262_263delinsGT MANE Select ENSP00000228606.4:p.Val88=
ENST00000228606.8:c.262_263delinsGT ENSP00000228606.4:p.Val88=
ENST00000546496.1:n.90_91delinsGT
ENST00000546609.1:c.174_175delinsGT
ENST00000547344.5:n.316_317delinsGT
ENST00000552186.1:n.381_382delinsGT
NM_000785.3:c.262_263delinsGT NP_000776.1:p.Val88=
NM_000785.4:c.262_263delinsGT MANE Select NP_000776.1:p.Val88=