Canonical Allele Identifier: CA1825496472

Gene: CYP11B1 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142875561_142875563delinsCCT , CM000670.2:g.142875561_142875563delinsCCT	GRCh38
NC_000008.10:g.143956977_143956979delinsCCT , CM000670.1:g.143956977_143956979delinsCCT	GRCh37
NC_000008.9:g.143953979_143953981delinsCCT	NCBI36
NG_007954.1:g.9258_9260delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.1121+149_1121+151delinsAGG (CYP11B1) MANE Select	ENSP00000292427.5:n.1121+149_1121+151delinsAGG
ENST00000292427.8:c.1121+149_1121+151delinsAGG (CYP11B1)	ENSP00000292427.4:n.1121+149_1121+151delinsAGG
ENST00000314111.4:n.1516+149_1516+151delinsAGG (CYP11B1)
ENST00000377675.3:c.1334+149_1334+151delinsAGG (CYP11B1)	ENSP00000366903.3:n.1334+149_1334+151delinsAGG
ENST00000517471.5:c.1121+149_1121+151delinsAGG (CYP11B1)	ENSP00000428043.1:n.1121+149_1121+151delinsAGG
ENST00000519285.5:c.86+149_86+151delinsAGG (CYP11B1)	ENSP00000430144.1:n.86+149_86+151delinsAGG
ENST00000522728.5:c.181+34336_181+34338delinsCCT (GML)	ENSP00000430799.1:n.181+34336_181+34338delinsCCT
NM_000497.3:c.1121+149_1121+151delinsAGG (CYP11B1)	NP_000488.3:n.1121+149_1121+151delinsAGG
NM_001026213.1:c.1121+149_1121+151delinsAGG (CYP11B1)	NP_001021384.1:n.1121+149_1121+151delinsAGG
XM_011516870.1:c.1199+149_1199+151delinsAGG (CYP11B1)	XP_011515172.1:n.1199+149_1199+151delinsAGG
XM_011516871.1:c.1199+149_1199+151delinsAGG (CYP11B1)	XP_011515173.1:n.1199+149_1199+151delinsAGG
XM_011516872.1:c.1121+149_1121+151delinsAGG (CYP11B1)	XP_011515174.1:n.1121+149_1121+151delinsAGG
XM_011516873.1:c.1199+149_1199+151delinsAGG (CYP11B1)	XP_011515175.1:n.1199+149_1199+151delinsAGG
XM_011516874.1:c.1199+149_1199+151delinsAGG (CYP11B1)	XP_011515176.1:n.1199+149_1199+151delinsAGG
XM_011516875.1:c.938+149_938+151delinsAGG (CYP11B1)	XP_011515177.1:n.938+149_938+151delinsAGG
XM_011516876.1:c.1199+149_1199+151delinsAGG (CYP11B1)	XP_011515178.1:n.1199+149_1199+151delinsAGG
XM_011516970.1:c.214+34336_214+34338delinsCCT (GML)	XP_011515272.1:n.214+34336_214+34338delinsCCT
NM_000497.4:c.1121+149_1121+151delinsAGG (CYP11B1) MANE Select	NP_000488.3:n.1121+149_1121+151delinsAGG