Canonical Allele Identifier: CA2688877057

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142875989_142875991del , CM000670.2:g.142875989_142875991del GRCh38
NC_000008.10:g.143957405_143957407del , CM000670.1:g.143957405_143957407del GRCh37
NC_000008.9:g.143954407_143954409del NCBI36
NG_007954.1:g.8830_8832del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292427.10:c.955-113_955-111del (CYP11B1) MANE Select ENSP00000292427.5:n.955-113_955-111del
ENST00000292427.8:c.955-113_955-111del (CYP11B1) ENSP00000292427.4:n.955-113_955-111del
ENST00000314111.4:n.1237_1239del (CYP11B1)
ENST00000377675.3:c.1168-113_1168-111del (CYP11B1) ENSP00000366903.3:n.1168-113_1168-111del
ENST00000517471.5:c.955-113_955-111del (CYP11B1) ENSP00000428043.1:n.955-113_955-111del
ENST00000522728.5:c.181+34764_181+34766del (GML) ENSP00000430799.1:n.181+34764_181+34766del
NM_000497.3:c.955-113_955-111del (CYP11B1) NP_000488.3:n.955-113_955-111del
NM_001026213.1:c.955-113_955-111del (CYP11B1) NP_001021384.1:n.955-113_955-111del
XM_011516870.1:c.1033-113_1033-111del (CYP11B1) XP_011515172.1:n.1033-113_1033-111del
XM_011516871.1:c.1033-113_1033-111del (CYP11B1) XP_011515173.1:n.1033-113_1033-111del
XM_011516872.1:c.955-113_955-111del (CYP11B1) XP_011515174.1:n.955-113_955-111del
XM_011516873.1:c.1033-113_1033-111del (CYP11B1) XP_011515175.1:n.1033-113_1033-111del
XM_011516874.1:c.1033-113_1033-111del (CYP11B1) XP_011515176.1:n.1033-113_1033-111del
XM_011516875.1:c.772-113_772-111del (CYP11B1) XP_011515177.1:n.772-113_772-111del
XM_011516876.1:c.1033-113_1033-111del (CYP11B1) XP_011515178.1:n.1033-113_1033-111del
XM_011516970.1:c.214+34764_214+34766del (GML) XP_011515272.1:n.214+34764_214+34766del
NM_000497.4:c.955-113_955-111del (CYP11B1) MANE Select NP_000488.3:n.955-113_955-111del