Canonical Allele Identifier: CA1825498680

Gene: CYP11B1 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142879061_142879064delinsATGT , CM000670.2:g.142879061_142879064delinsATGT	GRCh38
NC_000008.10:g.143960477_143960480delinsATGT , CM000670.1:g.143960477_143960480delinsATGT	GRCh37
NC_000008.9:g.143957479_143957482delinsATGT	NCBI36
NG_007954.1:g.5757_5760delinsACAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.363_366delinsACAT (CYP11B1) MANE Select	ENSP00000292427.5:p.Gln121=
ENST00000292427.8:c.363_366delinsACAT (CYP11B1)	ENSP00000292427.4:p.Gln121=
ENST00000314111.4:n.396_399delinsACAT (CYP11B1)
ENST00000377675.3:c.498_501delinsACAT (CYP11B1)	ENSP00000366903.3:p.Gln166=
ENST00000517471.5:c.363_366delinsACAT (CYP11B1)	ENSP00000428043.1:p.Gln121=
ENST00000522728.5:c.182-34902_182-34899delinsATGT (GML)	ENSP00000430799.1:n.182-34902_182-34899delinsATGT
NM_000497.3:c.363_366delinsACAT (CYP11B1)	NP_000488.3:p.Gln121=
NM_001026213.1:c.363_366delinsACAT (CYP11B1)	NP_001021384.1:p.Gln121=
XM_011516870.1:c.363_366delinsACAT (CYP11B1)	XP_011515172.1:p.Gln121=
XM_011516871.1:c.363_366delinsACAT (CYP11B1)	XP_011515173.1:p.Gln121=
XM_011516872.1:c.363_366delinsACAT (CYP11B1)	XP_011515174.1:p.Gln121=
XM_011516873.1:c.363_366delinsACAT (CYP11B1)	XP_011515175.1:p.Gln121=
XM_011516874.1:c.363_366delinsACAT (CYP11B1)	XP_011515176.1:p.Gln121=
XM_011516875.1:c.102_105delinsACAT (CYP11B1)	XP_011515177.1:p.Gln34=
XM_011516876.1:c.363_366delinsACAT (CYP11B1)	XP_011515178.1:p.Gln121=
XM_011516970.1:c.215-34902_215-34899delinsATGT (GML)	XP_011515272.1:n.215-34902_215-34899delinsATGT
NM_000497.4:c.363_366delinsACAT (CYP11B1) MANE Select	NP_000488.3:p.Gln121=