Canonical Allele Identifier: CA1825496767

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142876008_142876014delinsTCAAATC , CM000670.2:g.142876008_142876014delinsTCAAATC GRCh38
NC_000008.10:g.143957424_143957430delinsTCAAATC , CM000670.1:g.143957424_143957430delinsTCAAATC GRCh37
NC_000008.9:g.143954426_143954432delinsTCAAATC NCBI36
NG_007954.1:g.8807_8813delinsGATTTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000292427.10:c.955-136_955-130delinsGATTTGA (CYP11B1) MANE Select ENSP00000292427.5:n.955-136_955-130delinsGATTTGA
ENST00000292427.8:c.955-136_955-130delinsGATTTGA (CYP11B1) ENSP00000292427.4:n.955-136_955-130delinsGATTTGA
ENST00000314111.4:n.1214_1220delinsGATTTGA (CYP11B1)
ENST00000377675.3:c.1168-136_1168-130delinsGATTTGA (CYP11B1) ENSP00000366903.3:n.1168-136_1168-130delinsGATTTGA
ENST00000517471.5:c.955-136_955-130delinsGATTTGA (CYP11B1) ENSP00000428043.1:n.955-136_955-130delinsGATTTGA
ENST00000522728.5:c.181+34783_181+34789delinsTCAAATC (GML) ENSP00000430799.1:n.181+34783_181+34789delinsTCAAATC
NM_000497.3:c.955-136_955-130delinsGATTTGA (CYP11B1) NP_000488.3:n.955-136_955-130delinsGATTTGA
NM_001026213.1:c.955-136_955-130delinsGATTTGA (CYP11B1) NP_001021384.1:n.955-136_955-130delinsGATTTGA
XM_011516870.1:c.1033-136_1033-130delinsGATTTGA (CYP11B1) XP_011515172.1:n.1033-136_1033-130delinsGATTTGA
XM_011516871.1:c.1033-136_1033-130delinsGATTTGA (CYP11B1) XP_011515173.1:n.1033-136_1033-130delinsGATTTGA
XM_011516872.1:c.955-136_955-130delinsGATTTGA (CYP11B1) XP_011515174.1:n.955-136_955-130delinsGATTTGA
XM_011516873.1:c.1033-136_1033-130delinsGATTTGA (CYP11B1) XP_011515175.1:n.1033-136_1033-130delinsGATTTGA
XM_011516874.1:c.1033-136_1033-130delinsGATTTGA (CYP11B1) XP_011515176.1:n.1033-136_1033-130delinsGATTTGA
XM_011516875.1:c.772-136_772-130delinsGATTTGA (CYP11B1) XP_011515177.1:n.772-136_772-130delinsGATTTGA
XM_011516876.1:c.1033-136_1033-130delinsGATTTGA (CYP11B1) XP_011515178.1:n.1033-136_1033-130delinsGATTTGA
XM_011516970.1:c.214+34783_214+34789delinsTCAAATC (GML) XP_011515272.1:n.214+34783_214+34789delinsTCAAATC
NM_000497.4:c.955-136_955-130delinsGATTTGA (CYP11B1) MANE Select NP_000488.3:n.955-136_955-130delinsGATTTGA