Canonical Allele Identifier: CA2688877184

Gene: CYP11B1 GML

Linked Data

• gnomAD v4: 8-142876056-A-AGG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142876056_142876057insGG , CM000670.2:g.142876056_142876057insGG	GRCh38
NC_000008.10:g.143957472_143957473insGG , CM000670.1:g.143957472_143957473insGG	GRCh37
NC_000008.9:g.143954474_143954475insGG	NCBI36
NG_007954.1:g.8764_8765insCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000292427.10:c.955-179_955-178insCC (CYP11B1) MANE Select	ENSP00000292427.5:n.955-179_955-178insCC
ENST00000292427.8:c.955-179_955-178insCC (CYP11B1)	ENSP00000292427.4:n.955-179_955-178insCC
ENST00000314111.4:n.1171_1172insCC (CYP11B1)
ENST00000377675.3:c.1168-179_1168-178insCC (CYP11B1)	ENSP00000366903.3:n.1168-179_1168-178insCC
ENST00000517471.5:c.955-179_955-178insCC (CYP11B1)	ENSP00000428043.1:n.955-179_955-178insCC
ENST00000522728.5:c.181+34831_181+34832insGG (GML)	ENSP00000430799.1:n.181+34831_181+34832insGG
NM_000497.3:c.955-179_955-178insCC (CYP11B1)	NP_000488.3:n.955-179_955-178insCC
NM_001026213.1:c.955-179_955-178insCC (CYP11B1)	NP_001021384.1:n.955-179_955-178insCC
XM_011516870.1:c.1033-179_1033-178insCC (CYP11B1)	XP_011515172.1:n.1033-179_1033-178insCC
XM_011516871.1:c.1033-179_1033-178insCC (CYP11B1)	XP_011515173.1:n.1033-179_1033-178insCC
XM_011516872.1:c.955-179_955-178insCC (CYP11B1)	XP_011515174.1:n.955-179_955-178insCC
XM_011516873.1:c.1033-179_1033-178insCC (CYP11B1)	XP_011515175.1:n.1033-179_1033-178insCC
XM_011516874.1:c.1033-179_1033-178insCC (CYP11B1)	XP_011515176.1:n.1033-179_1033-178insCC
XM_011516875.1:c.772-179_772-178insCC (CYP11B1)	XP_011515177.1:n.772-179_772-178insCC
XM_011516876.1:c.1033-179_1033-178insCC (CYP11B1)	XP_011515178.1:n.1033-179_1033-178insCC
XM_011516970.1:c.214+34831_214+34832insGG (GML)	XP_011515272.1:n.214+34831_214+34832insGG
NM_000497.4:c.955-179_955-178insCC (CYP11B1) MANE Select	NP_000488.3:n.955-179_955-178insCC