Canonical Allele Identifier: CA2674265080

Gene: HMGCR CERT1

Linked Data

• gnomAD v4: 5-75359766-C-CATGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.75359766_75359767insATGTT , CM000667.2:g.75359766_75359767insATGTT	GRCh38
NC_000005.9:g.74655591_74655592insATGTT , CM000667.1:g.74655591_74655592insATGTT	GRCh37
NC_000005.8:g.74691347_74691348insATGTT	NCBI36
NG_011449.1:g.27599_27600insATGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287936.9:c.2457+210_2457+211insATGTT (HMGCR) MANE Select	ENSP00000287936.4:n.2457+210_2457+211insATGTT
ENST00000644912.1:c.1670-2755_1670-2754insAACAT (CERT1)	ENSP00000495172.1:n.1670-2755_1670-2754insAACAT
ENST00000646172.1:c.1203-2755_1203-2754insAACAT (CERT1)	ENSP00000494969.1:n.1203-2755_1203-2754insAACAT
ENST00000679456.1:n.3294+210_3294+211insATGTT (HMGCR)
ENST00000680160.1:c.2413-219_2413-218insATGTT (HMGCR)	ENSP00000505315.1:n.2413-219_2413-218insATGTT
ENST00000680940.1:c.2457+210_2457+211insATGTT (HMGCR)	ENSP00000505561.1:n.2457+210_2457+211insATGTT
ENST00000681271.1:c.2457+210_2457+211insATGTT (HMGCR)	ENSP00000505805.1:n.2457+210_2457+211insATGTT
ENST00000681410.1:c.2457+210_2457+211insATGTT (HMGCR)	ENSP00000506232.1:n.2457+210_2457+211insATGTT
ENST00000681567.1:c.*3006+210_*3006+211insATGTT (HMGCR)	ENSP00000506708.1:n.*3006+210_*3006+211insATGTT
ENST00000287936.8:c.2457+210_2457+211insATGTT (HMGCR)	ENSP00000287936.4:n.2457+210_2457+211insATGTT
ENST00000343975.9:c.2298+210_2298+211insATGTT (HMGCR)	ENSP00000340816.5:n.2298+210_2298+211insATGTT
ENST00000509085.5:c.288-219_288-218insATGTT (HMGCR)
ENST00000511206.5:c.2457+210_2457+211insATGTT (HMGCR)	ENSP00000426745.1:n.2457+210_2457+211insATGTT
ENST00000511986.1:c.139-219_139-218insATGTT (HMGCR)	ENSP00000420871.1:n.139-219_139-218insATGTT
NM_000859.2:c.2457+210_2457+211insATGTT (HMGCR)	NP_000850.1:n.2457+210_2457+211insATGTT
NM_001130996.1:c.2298+210_2298+211insATGTT (HMGCR)	NP_001124468.1:n.2298+210_2298+211insATGTT
XM_011543357.1:c.2517+210_2517+211insATGTT (HMGCR)	XP_011541659.1:n.2517+210_2517+211insATGTT
XM_011543358.1:c.2457+210_2457+211insATGTT (HMGCR)	XP_011541660.1:n.2457+210_2457+211insATGTT
XM_011543359.1:c.2358+210_2358+211insATGTT (HMGCR)	XP_011541661.1:n.2358+210_2358+211insATGTT
NM_001364187.1:c.2457+210_2457+211insATGTT (HMGCR)	NP_001351116.1:n.2457+210_2457+211insATGTT
NM_000859.3:c.2457+210_2457+211insATGTT (HMGCR) MANE Select	NP_000850.1:n.2457+210_2457+211insATGTT
NM_001130996.2:c.2298+210_2298+211insATGTT (HMGCR)	NP_001124468.1:n.2298+210_2298+211insATGTT