Canonical Allele Identifier: CA2688877561

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142876468_142876476del , CM000670.2:g.142876468_142876476del GRCh38
NC_000008.10:g.143957884_143957892del , CM000670.1:g.143957884_143957892del GRCh37
NC_000008.9:g.143954886_143954894del NCBI36
NG_007954.1:g.8351_8359del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292427.10:c.800-75_800-67del (CYP11B1) MANE Select ENSP00000292427.5:n.800-75_800-67del
ENST00000292427.8:c.800-75_800-67del (CYP11B1) ENSP00000292427.4:n.800-75_800-67del
ENST00000314111.4:n.833-75_833-67del (CYP11B1)
ENST00000377675.3:c.1013-75_1013-67del (CYP11B1) ENSP00000366903.3:n.1013-75_1013-67del
ENST00000517471.5:c.800-75_800-67del (CYP11B1) ENSP00000428043.1:n.800-75_800-67del
ENST00000522728.5:c.181+35243_181+35251del (GML) ENSP00000430799.1:n.181+35243_181+35251del
NM_000497.3:c.800-75_800-67del (CYP11B1) NP_000488.3:n.800-75_800-67del
NM_001026213.1:c.800-75_800-67del (CYP11B1) NP_001021384.1:n.800-75_800-67del
XM_011516870.1:c.878-75_878-67del (CYP11B1) XP_011515172.1:n.878-75_878-67del
XM_011516871.1:c.878-75_878-67del (CYP11B1) XP_011515173.1:n.878-75_878-67del
XM_011516872.1:c.800-75_800-67del (CYP11B1) XP_011515174.1:n.800-75_800-67del
XM_011516873.1:c.878-75_878-67del (CYP11B1) XP_011515175.1:n.878-75_878-67del
XM_011516874.1:c.878-75_878-67del (CYP11B1) XP_011515176.1:n.878-75_878-67del
XM_011516875.1:c.617-75_617-67del (CYP11B1) XP_011515177.1:n.617-75_617-67del
XM_011516876.1:c.878-75_878-67del (CYP11B1) XP_011515178.1:n.878-75_878-67del
XM_011516970.1:c.214+35243_214+35251del (GML) XP_011515272.1:n.214+35243_214+35251del
NM_000497.4:c.800-75_800-67del (CYP11B1) MANE Select NP_000488.3:n.800-75_800-67del