Canonical Allele Identifier: CA1825496772

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142876020_142876021delinsGC , CM000670.2:g.142876020_142876021delinsGC GRCh38
NC_000008.10:g.143957436_143957437delinsGC , CM000670.1:g.143957436_143957437delinsGC GRCh37
NC_000008.9:g.143954438_143954439delinsGC NCBI36
NG_007954.1:g.8800_8801delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000292427.10:c.955-143_955-142delinsGC (CYP11B1) MANE Select ENSP00000292427.5:n.955-143_955-142delinsGC
ENST00000292427.8:c.955-143_955-142delinsGC (CYP11B1) ENSP00000292427.4:n.955-143_955-142delinsGC
ENST00000314111.4:n.1207_1208delinsGC (CYP11B1)
ENST00000377675.3:c.1168-143_1168-142delinsGC (CYP11B1) ENSP00000366903.3:n.1168-143_1168-142delinsGC
ENST00000517471.5:c.955-143_955-142delinsGC (CYP11B1) ENSP00000428043.1:n.955-143_955-142delinsGC
ENST00000522728.5:c.181+34795_181+34796delinsGC (GML) ENSP00000430799.1:n.181+34795_181+34796delinsGC
NM_000497.3:c.955-143_955-142delinsGC (CYP11B1) NP_000488.3:n.955-143_955-142delinsGC
NM_001026213.1:c.955-143_955-142delinsGC (CYP11B1) NP_001021384.1:n.955-143_955-142delinsGC
XM_011516870.1:c.1033-143_1033-142delinsGC (CYP11B1) XP_011515172.1:n.1033-143_1033-142delinsGC
XM_011516871.1:c.1033-143_1033-142delinsGC (CYP11B1) XP_011515173.1:n.1033-143_1033-142delinsGC
XM_011516872.1:c.955-143_955-142delinsGC (CYP11B1) XP_011515174.1:n.955-143_955-142delinsGC
XM_011516873.1:c.1033-143_1033-142delinsGC (CYP11B1) XP_011515175.1:n.1033-143_1033-142delinsGC
XM_011516874.1:c.1033-143_1033-142delinsGC (CYP11B1) XP_011515176.1:n.1033-143_1033-142delinsGC
XM_011516875.1:c.772-143_772-142delinsGC (CYP11B1) XP_011515177.1:n.772-143_772-142delinsGC
XM_011516876.1:c.1033-143_1033-142delinsGC (CYP11B1) XP_011515178.1:n.1033-143_1033-142delinsGC
XM_011516970.1:c.214+34795_214+34796delinsGC (GML) XP_011515272.1:n.214+34795_214+34796delinsGC
NM_000497.4:c.955-143_955-142delinsGC (CYP11B1) MANE Select NP_000488.3:n.955-143_955-142delinsGC