Canonical Allele Identifier: CA1328916178

Gene: CYP27A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218782308A= , CM000664.2:g.218782308A=	GRCh38
NC_000002.11:g.219647031A= , CM000664.1:g.219647031A=	GRCh37
NC_000002.10:g.219355275A=	NCBI36
NG_007959.1:g.5560A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258415.9:c.126A= MANE Select	ENSP00000258415.4:p.Gly42=
ENST00000258415.8:c.126A=	ENSP00000258415.4:p.Gly42=
ENST00000445971.1:c.126A=	ENSP00000404945.1:p.Gly42=
ENST00000466602.1:n.135A=
ENST00000494263.5:n.560A=
NM_000784.3:c.126A=	NP_000775.1:p.Gly42=
XM_017003488.2:c.-104A=	XP_016858977.1:n.-104A=
NM_000784.4:c.126A= MANE Select	NP_000775.1:p.Gly42=