Canonical Allele Identifier: CA1825497037

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142876453_142876456delinsGTCC , CM000670.2:g.142876453_142876456delinsGTCC GRCh38
NC_000008.10:g.143957869_143957872delinsGTCC , CM000670.1:g.143957869_143957872delinsGTCC GRCh37
NC_000008.9:g.143954871_143954874delinsGTCC NCBI36
NG_007954.1:g.8365_8368delinsGGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000292427.10:c.800-61_800-58delinsGGAC (CYP11B1) MANE Select ENSP00000292427.5:n.800-61_800-58delinsGGAC
ENST00000292427.8:c.800-61_800-58delinsGGAC (CYP11B1) ENSP00000292427.4:n.800-61_800-58delinsGGAC
ENST00000314111.4:n.833-61_833-58delinsGGAC (CYP11B1)
ENST00000377675.3:c.1013-61_1013-58delinsGGAC (CYP11B1) ENSP00000366903.3:n.1013-61_1013-58delinsGGAC
ENST00000517471.5:c.800-61_800-58delinsGGAC (CYP11B1) ENSP00000428043.1:n.800-61_800-58delinsGGAC
ENST00000522728.5:c.181+35228_181+35231delinsGTCC (GML) ENSP00000430799.1:n.181+35228_181+35231delinsGTCC
NM_000497.3:c.800-61_800-58delinsGGAC (CYP11B1) NP_000488.3:n.800-61_800-58delinsGGAC
NM_001026213.1:c.800-61_800-58delinsGGAC (CYP11B1) NP_001021384.1:n.800-61_800-58delinsGGAC
XM_011516870.1:c.878-61_878-58delinsGGAC (CYP11B1) XP_011515172.1:n.878-61_878-58delinsGGAC
XM_011516871.1:c.878-61_878-58delinsGGAC (CYP11B1) XP_011515173.1:n.878-61_878-58delinsGGAC
XM_011516872.1:c.800-61_800-58delinsGGAC (CYP11B1) XP_011515174.1:n.800-61_800-58delinsGGAC
XM_011516873.1:c.878-61_878-58delinsGGAC (CYP11B1) XP_011515175.1:n.878-61_878-58delinsGGAC
XM_011516874.1:c.878-61_878-58delinsGGAC (CYP11B1) XP_011515176.1:n.878-61_878-58delinsGGAC
XM_011516875.1:c.617-61_617-58delinsGGAC (CYP11B1) XP_011515177.1:n.617-61_617-58delinsGGAC
XM_011516876.1:c.878-61_878-58delinsGGAC (CYP11B1) XP_011515178.1:n.878-61_878-58delinsGGAC
XM_011516970.1:c.214+35228_214+35231delinsGTCC (GML) XP_011515272.1:n.214+35228_214+35231delinsGTCC
NM_000497.4:c.800-61_800-58delinsGGAC (CYP11B1) MANE Select NP_000488.3:n.800-61_800-58delinsGGAC