Canonical Allele Identifier: CA2688876969

Gene: CYP11B1 GML

Linked Data

• gnomAD v4: 8-142875662-G-GCT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142875666_142875667dup , CM000670.2:g.142875666_142875667dup	GRCh38
NC_000008.10:g.143957082_143957083dup , CM000670.1:g.143957082_143957083dup	GRCh37
NC_000008.9:g.143954084_143954085dup	NCBI36
NG_007954.1:g.9157_9158dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000292427.10:c.1121+48_1121+49dup (CYP11B1) MANE Select	ENSP00000292427.5:n.1121+48_1121+49dup
ENST00000292427.8:c.1121+48_1121+49dup (CYP11B1)	ENSP00000292427.4:n.1121+48_1121+49dup
ENST00000314111.4:n.1516+48_1516+49dup (CYP11B1)
ENST00000377675.3:c.1334+48_1334+49dup (CYP11B1)	ENSP00000366903.3:n.1334+48_1334+49dup
ENST00000517471.5:c.1121+48_1121+49dup (CYP11B1)	ENSP00000428043.1:n.1121+48_1121+49dup
ENST00000519285.5:c.86+48_86+49dup (CYP11B1)	ENSP00000430144.1:n.86+48_86+49dup
ENST00000522728.5:c.181+34441_181+34442dup (GML)	ENSP00000430799.1:n.181+34441_181+34442du...
NM_000497.3:c.1121+48_1121+49dup (CYP11B1)	NP_000488.3:n.1121+48_1121+49dup
NM_001026213.1:c.1121+48_1121+49dup (CYP11B1)	NP_001021384.1:n.1121+48_1121+49dup
XM_011516870.1:c.1199+48_1199+49dup (CYP11B1)	XP_011515172.1:n.1199+48_1199+49dup
XM_011516871.1:c.1199+48_1199+49dup (CYP11B1)	XP_011515173.1:n.1199+48_1199+49dup
XM_011516872.1:c.1121+48_1121+49dup (CYP11B1)	XP_011515174.1:n.1121+48_1121+49dup
XM_011516873.1:c.1199+48_1199+49dup (CYP11B1)	XP_011515175.1:n.1199+48_1199+49dup
XM_011516874.1:c.1199+48_1199+49dup (CYP11B1)	XP_011515176.1:n.1199+48_1199+49dup
XM_011516875.1:c.938+48_938+49dup (CYP11B1)	XP_011515177.1:n.938+48_938+49dup
XM_011516876.1:c.1199+48_1199+49dup (CYP11B1)	XP_011515178.1:n.1199+48_1199+49dup
XM_011516970.1:c.214+34441_214+34442dup (GML)	XP_011515272.1:n.214+34441_214+34442dup
NM_000497.4:c.1121+48_1121+49dup (CYP11B1) MANE Select	NP_000488.3:n.1121+48_1121+49dup