Canonical Allele Identifier: CA1825495796

Gene: CYP11B1 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142874446_142874447delinsTC , CM000670.2:g.142874446_142874447delinsTC	GRCh38
NC_000008.10:g.143955862_143955863delinsTC , CM000670.1:g.143955862_143955863delinsTC	GRCh37
NC_000008.9:g.143952864_143952865delinsTC	NCBI36
NG_007954.1:g.10374_10375delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000292427.10:c.1438_1439delinsGA (CYP11B1) MANE Select	ENSP00000292427.5:p.Asp480=
ENST00000292427.8:c.1438_1439delinsGA (CYP11B1)	ENSP00000292427.4:p.Asp480=
ENST00000314111.4:n.1635_1636delinsGA (CYP11B1)
ENST00000377675.3:c.1651_1652delinsGA (CYP11B1)	ENSP00000366903.3:p.Asp551=
ENST00000517471.5:c.1240_1241delinsGA (CYP11B1)	ENSP00000428043.1:p.Asp414=
ENST00000519285.5:c.472_473delinsGA (CYP11B1)	ENSP00000430144.1:p.Asp158=
ENST00000522728.5:c.181+33221_181+33222delinsTC (GML)	ENSP00000430799.1:n.181+33221_181+33222de...
NM_000497.3:c.1438_1439delinsGA (CYP11B1)	NP_000488.3:p.Asp480=
NM_001026213.1:c.1240_1241delinsGA (CYP11B1)	NP_001021384.1:p.Asp414=
XM_011516870.1:c.1676_1677delinsGA (CYP11B1)	XP_011515172.1:p.Gly559=
XM_011516871.1:c.1607_1608delinsGA (CYP11B1)	XP_011515173.1:p.Gly536=
XM_011516872.1:c.1598_1599delinsGA (CYP11B1)	XP_011515174.1:p.Gly533=
XM_011516873.1:c.1585_1586delinsGA (CYP11B1)	XP_011515175.1:p.Asp529=
XM_011516874.1:c.1516_1517delinsGA (CYP11B1)	XP_011515176.1:p.Asp506=
XM_011516875.1:c.1415_1416delinsGA (CYP11B1)	XP_011515177.1:p.Gly472=
XM_011516876.1:c.1387_1388delinsGA (CYP11B1)	XP_011515178.1:p.Asp463=
XM_011516970.1:c.214+33221_214+33222delinsTC (GML)	XP_011515272.1:n.214+33221_214+33222delin...
NM_000497.4:c.1438_1439delinsGA (CYP11B1) MANE Select	NP_000488.3:p.Asp480=