Canonical Allele Identifier: CA1825496321

Gene: CYP11B1 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142875340G= , CM000670.2:g.142875340G=	GRCh38
NC_000008.10:g.143956756G= , CM000670.1:g.143956756G=	GRCh37
NC_000008.9:g.143953758G=	NCBI36
NG_007954.1:g.9481C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.1122-28C= (CYP11B1) MANE Select	ENSP00000292427.5:n.1122-28C=
ENST00000292427.8:c.1122-28C= (CYP11B1)	ENSP00000292427.4:n.1122-28C=
ENST00000314111.4:n.1517-28C= (CYP11B1)
ENST00000377675.3:c.1335-28C= (CYP11B1)	ENSP00000366903.3:n.1335-28C=
ENST00000517471.5:c.1122-28C= (CYP11B1)	ENSP00000428043.1:n.1122-28C=
ENST00000519285.5:c.128C= (CYP11B1)	ENSP00000430144.1:p.Thr43=
ENST00000522728.5:c.181+34115G= (GML)	ENSP00000430799.1:n.181+34115G=
NM_000497.3:c.1122-28C= (CYP11B1)	NP_000488.3:n.1122-28C=
NM_001026213.1:c.1122-28C= (CYP11B1)	NP_001021384.1:n.1122-28C=
XM_011516870.1:c.1241C= (CYP11B1)	XP_011515172.1:p.Thr414=
XM_011516871.1:c.1200-28C= (CYP11B1)	XP_011515173.1:n.1200-28C=
XM_011516872.1:c.1163C= (CYP11B1)	XP_011515174.1:p.Thr388=
XM_011516873.1:c.1241C= (CYP11B1)	XP_011515175.1:p.Thr414=
XM_011516874.1:c.1200-28C= (CYP11B1)	XP_011515176.1:n.1200-28C=
XM_011516875.1:c.980C= (CYP11B1)	XP_011515177.1:p.Thr327=
XM_011516876.1:c.1241C= (CYP11B1)	XP_011515178.1:p.Thr414=
XM_011516970.1:c.214+34115G= (GML)	XP_011515272.1:n.214+34115G=
NM_000497.4:c.1122-28C= (CYP11B1) MANE Select	NP_000488.3:n.1122-28C=