Canonical Allele Identifier: CA1556072244

Gene: HMGCR CERT1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.75356374A= , CM000667.2:g.75356374A=	GRCh38
NC_000005.9:g.74652199A= , CM000667.1:g.74652199A=	GRCh37
NC_000005.8:g.74687955A=	NCBI36
NG_011449.1:g.24207A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287936.9:c.1912A= (HMGCR) MANE Select	ENSP00000287936.4:p.Ile638=
ENST00000644912.1:c.*553T= (CERT1)	ENSP00000495172.1:n.*553T=
ENST00000646172.1:c.1841T= (CERT1)	ENSP00000494969.1:n.1841T=
ENST00000679456.1:n.2749A= (HMGCR)
ENST00000680160.1:c.1912A= (HMGCR)	ENSP00000505315.1:p.Ile638=
ENST00000680940.1:c.1912A= (HMGCR)	ENSP00000505561.1:p.Ile638=
ENST00000681271.1:c.1912A= (HMGCR)	ENSP00000505805.1:p.Ile638=
ENST00000681410.1:c.1912A= (HMGCR)	ENSP00000506232.1:p.Ile638=
ENST00000681567.1:c.*2461A= (HMGCR)	ENSP00000506708.1:n.*2461A=
ENST00000287936.8:c.1912A= (HMGCR)	ENSP00000287936.4:p.Ile638=
ENST00000343975.9:c.1753A= (HMGCR)	ENSP00000340816.5:p.Ile585=
ENST00000508070.1:n.375A= (HMGCR)
ENST00000511206.5:c.1912A= (HMGCR)	ENSP00000426745.1:p.Ile638=
NM_000859.2:c.1912A= (HMGCR)	NP_000850.1:p.Ile638=
NM_001130996.1:c.1753A= (HMGCR)	NP_001124468.1:p.Ile585=
XM_011543357.1:c.1972A= (HMGCR)	XP_011541659.1:p.Ile658=
XM_011543358.1:c.1912A= (HMGCR)	XP_011541660.1:p.Ile638=
XM_011543359.1:c.1813A= (HMGCR)	XP_011541661.1:p.Ile605=
NM_001364187.1:c.1912A= (HMGCR)	NP_001351116.1:p.Ile638=
NM_000859.3:c.1912A= (HMGCR) MANE Select	NP_000850.1:p.Ile638=
NM_001130996.2:c.1753A= (HMGCR)	NP_001124468.1:p.Ile585=