Canonical Allele Identifier: CA585726636

Linked Data

dbSNP Id: rs1202367234

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142875378del , CM000670.2:g.142875378del GRCh38
NC_000008.10:g.143956794del , CM000670.1:g.143956794del GRCh37
NC_000008.9:g.143953796del NCBI36
NG_007954.1:g.9445del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292427.10:c.1122-64del (CYP11B1) MANE Select ENSP00000292427.5:n.1122-64del
ENST00000292427.8:c.1122-64del (CYP11B1) ENSP00000292427.4:n.1122-64del
ENST00000314111.4:n.1517-64del (CYP11B1)
ENST00000377675.3:c.1335-64del (CYP11B1) ENSP00000366903.3:n.1335-64del
ENST00000517471.5:c.1122-64del (CYP11B1) ENSP00000428043.1:n.1122-64del
ENST00000519285.5:c.92del (CYP11B1) ENSP00000430144.1:p.Gly31ValfsTer11
ENST00000522728.5:c.181+34153del (GML) ENSP00000430799.1:n.181+34153del
NM_000497.3:c.1122-64del (CYP11B1) NP_000488.3:n.1122-64del
NM_001026213.1:c.1122-64del (CYP11B1) NP_001021384.1:n.1122-64del
XM_011516870.1:c.1205del (CYP11B1) XP_011515172.1:p.Gly402ValfsTer11
XM_011516871.1:c.1200-64del (CYP11B1) XP_011515173.1:n.1200-64del
XM_011516872.1:c.1127del (CYP11B1) XP_011515174.1:p.Gly376ValfsTer11
XM_011516873.1:c.1205del (CYP11B1) XP_011515175.1:p.Gly402ValfsTer11
XM_011516874.1:c.1200-64del (CYP11B1) XP_011515176.1:n.1200-64del
XM_011516875.1:c.944del (CYP11B1) XP_011515177.1:p.Gly315ValfsTer11
XM_011516876.1:c.1205del (CYP11B1) XP_011515178.1:p.Gly402ValfsTer11
XM_011516970.1:c.214+34153del (GML) XP_011515272.1:n.214+34153del
NM_000497.4:c.1122-64del (CYP11B1) MANE Select NP_000488.3:n.1122-64del