Canonical Allele Identifier: CA2619519433
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57766031_57766037del , CM000674.2:g.57766031_57766037del GRCh38
NC_000012.11:g.58159814_58159820del , CM000674.1:g.58159814_58159820del GRCh37
NC_000012.10:g.56446081_56446087del NCBI36
NG_007076.1:g.6159_6165del

Transcript Alleles

HGVS Amino-acid change
ENST00000546609.2:n.270_276del
ENST00000713544.1:c.358_364del ENSP00000518840.1:p.Arg120GlyfsTer?
ENST00000713545.1:c.358_364del ENSP00000518841.1:p.Arg120GlyfsTer?
ENST00000228606.9:c.358_364del MANE Select ENSP00000228606.4:p.Arg120GlyfsTer?
ENST00000228606.8:c.358_364del ENSP00000228606.4:p.Arg120GlyfsTer?
ENST00000546496.1:n.186_192del
ENST00000546609.1:c.270_276del
ENST00000547344.5:n.412_418del
ENST00000552186.1:n.477_483del
NM_000785.3:c.358_364del NP_000776.1:p.Arg120GlyfsTer?
NM_000785.4:c.358_364del MANE Select NP_000776.1:p.Arg120GlyfsTer?