Canonical Allele Identifier: CA2039016296

Gene: CYP27B1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57764137G= , CM000674.2:g.57764137G=	GRCh38
NC_000012.11:g.58157920G= , CM000674.1:g.58157920G=	GRCh37
NC_000012.10:g.56444187G=	NCBI36
NG_007076.1:g.8057C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713544.1:c.1257C=	ENSP00000518840.1:p.Asp419=
ENST00000713545.1:c.*181C=	ENSP00000518841.1:n.*181C=
ENST00000228606.9:c.1176C= MANE Select	ENSP00000228606.4:p.Asp392=
ENST00000228606.8:c.1176C=	ENSP00000228606.4:p.Asp392=
ENST00000546567.5:c.471C=	ENSP00000449472.1:p.Asp157=
ENST00000547344.5:n.1315C=
NM_000785.3:c.1176C=	NP_000776.1:p.Asp392=
NM_000785.4:c.1176C= MANE Select	NP_000776.1:p.Asp392=