Canonical Allele Identifier: CA1825496137

Gene: CYP11B1 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142875012C= , CM000670.2:g.142875012C=	GRCh38
NC_000008.10:g.143956428C= , CM000670.1:g.143956428C=	GRCh37
NC_000008.9:g.143953430C=	NCBI36
NG_007954.1:g.9809G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000497.4:c.1343G= (CYP11B1) MANE Select	NP_000488.3:p.Arg448=
ENST00000292427.10:c.1343G= (CYP11B1) MANE Select	ENSP00000292427.5:p.Arg448=
NM_000497.3:c.1343G= (CYP11B1)	NP_000488.3:p.Arg448=
NM_001026213.1:c.1200+222G= (CYP11B1)	NP_001021384.1:n.1200+222G=
ENST00000292427.8:c.1343G= (CYP11B1)	ENSP00000292427.4:p.Arg448=
ENST00000314111.4:n.1595+222G= (CYP11B1)
ENST00000377675.3:c.1556G= (CYP11B1)	ENSP00000366903.3:p.Arg519=
ENST00000517471.5:c.1200+222G= (CYP11B1)	ENSP00000428043.1:n.1200+222G=
ENST00000519285.5:c.377G= (CYP11B1)	ENSP00000430144.1:p.Arg126=
ENST00000522728.5:c.181+33787C= (GML)	ENSP00000430799.1:n.181+33787C=
XM_011516870.1:c.1490G= (CYP11B1)	XP_011515172.1:p.Arg497=
XM_011516871.1:c.1421G= (CYP11B1)	XP_011515173.1:p.Arg474=
XM_011516872.1:c.1412G= (CYP11B1)	XP_011515174.1:p.Arg471=
XM_011516873.1:c.1490G= (CYP11B1)	XP_011515175.1:p.Arg497=
XM_011516874.1:c.1421G= (CYP11B1)	XP_011515176.1:p.Arg474=
XM_011516875.1:c.1229G= (CYP11B1)	XP_011515177.1:p.Arg410=
XM_011516876.1:c.1347+222G= (CYP11B1)	XP_011515178.1:n.1347+222G=
XM_011516970.1:c.214+33787C= (GML)	XP_011515272.1:n.214+33787C=