Canonical Allele Identifier: CA2688876992

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142875740del , CM000670.2:g.142875740del GRCh38
NC_000008.10:g.143957156del , CM000670.1:g.143957156del GRCh37
NC_000008.9:g.143954158del NCBI36
NG_007954.1:g.9081del

Transcript Alleles

HGVS Amino-acid change
ENST00000292427.10:c.1093del (CYP11B1) MANE Select ENSP00000292427.5:p.Leu365CysfsTer?
ENST00000292427.8:c.1093del (CYP11B1) ENSP00000292427.4:p.Leu365CysfsTer?
ENST00000314111.4:n.1488del (CYP11B1)
ENST00000377675.3:c.1306del (CYP11B1) ENSP00000366903.3:p.Leu436CysfsTer?
ENST00000517471.5:c.1093del (CYP11B1) ENSP00000428043.1:p.Leu365CysfsTer?
ENST00000519285.5:c.58del (CYP11B1) ENSP00000430144.1:p.Leu20CysfsTer22
ENST00000522728.5:c.181+34515del (GML) ENSP00000430799.1:n.181+34515del
NM_000497.3:c.1093del (CYP11B1) NP_000488.3:p.Leu365CysfsTer?
NM_001026213.1:c.1093del (CYP11B1) NP_001021384.1:p.Leu365CysfsTer?
XM_011516870.1:c.1171del (CYP11B1) XP_011515172.1:p.Leu391CysfsTer22
XM_011516871.1:c.1171del (CYP11B1) XP_011515173.1:p.Leu391CysfsTer?
XM_011516872.1:c.1093del (CYP11B1) XP_011515174.1:p.Leu365CysfsTer22
XM_011516873.1:c.1171del (CYP11B1) XP_011515175.1:p.Leu391CysfsTer22
XM_011516874.1:c.1171del (CYP11B1) XP_011515176.1:p.Leu391CysfsTer?
XM_011516875.1:c.910del (CYP11B1) XP_011515177.1:p.Leu304CysfsTer22
XM_011516876.1:c.1171del (CYP11B1) XP_011515178.1:p.Leu391CysfsTer22
XM_011516970.1:c.214+34515del (GML) XP_011515272.1:n.214+34515del
NM_000497.4:c.1093del (CYP11B1) MANE Select NP_000488.3:p.Leu365CysfsTer?