Canonical Allele Identifier: CA1556068563

Gene: HMGCR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.75352456G= , CM000667.2:g.75352456G=	GRCh38
NC_000005.9:g.74648281G= , CM000667.1:g.74648281G=	GRCh37
NC_000005.8:g.74684037G=	NCBI36
NG_011449.1:g.20289G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287936.9:c.1368+854G= MANE Select	ENSP00000287936.4:n.1368+854G=
ENST00000679456.1:n.2205+854G=
ENST00000680160.1:c.1368+854G=	ENSP00000505315.1:n.1368+854G=
ENST00000680940.1:c.1368+854G=	ENSP00000505561.1:n.1368+854G=
ENST00000681271.1:c.1368+854G=	ENSP00000505805.1:n.1368+854G=
ENST00000681410.1:c.1368+854G=	ENSP00000506232.1:n.1368+854G=
ENST00000681567.1:c.*1917+854G=	ENSP00000506708.1:n.*1917+854G=
ENST00000287936.8:c.1368+854G=	ENSP00000287936.4:n.1368+854G=
ENST00000343975.9:c.1368+854G=	ENSP00000340816.5:n.1368+854G=
ENST00000511206.5:c.1368+854G=	ENSP00000426745.1:n.1368+854G=
NM_000859.2:c.1368+854G=	NP_000850.1:n.1368+854G=
NM_001130996.1:c.1368+854G=	NP_001124468.1:n.1368+854G=
XM_011543357.1:c.1428+854G=	XP_011541659.1:n.1428+854G=
XM_011543358.1:c.1368+854G=	XP_011541660.1:n.1368+854G=
XM_011543359.1:c.1428+854G=	XP_011541661.1:n.1428+854G=
NM_001364187.1:c.1368+854G=	NP_001351116.1:n.1368+854G=
NM_000859.3:c.1368+854G= MANE Select	NP_000850.1:n.1368+854G=
NM_001130996.2:c.1368+854G=	NP_001124468.1:n.1368+854G=