Canonical Allele Identifier: CA1825496511

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142875634_142875636delinsTTC , CM000670.2:g.142875634_142875636delinsTTC GRCh38
NC_000008.10:g.143957050_143957052delinsTTC , CM000670.1:g.143957050_143957052delinsTTC GRCh37
NC_000008.9:g.143954052_143954054delinsTTC NCBI36
NG_007954.1:g.9185_9187delinsGAA

Transcript Alleles

HGVS Amino-acid change
ENST00000292427.10:c.1121+76_1121+78delinsGAA (CYP11B1) MANE Select ENSP00000292427.5:n.1121+76_1121+78delins...
ENST00000292427.8:c.1121+76_1121+78delinsGAA (CYP11B1) ENSP00000292427.4:n.1121+76_1121+78delins...
ENST00000314111.4:n.1516+76_1516+78delinsGAA (CYP11B1)
ENST00000377675.3:c.1334+76_1334+78delinsGAA (CYP11B1) ENSP00000366903.3:n.1334+76_1334+78delins...
ENST00000517471.5:c.1121+76_1121+78delinsGAA (CYP11B1) ENSP00000428043.1:n.1121+76_1121+78delins...
ENST00000519285.5:c.86+76_86+78delinsGAA (CYP11B1) ENSP00000430144.1:n.86+76_86+78delinsGAA
ENST00000522728.5:c.181+34409_181+34411delinsTTC (GML) ENSP00000430799.1:n.181+34409_181+34411de...
NM_000497.3:c.1121+76_1121+78delinsGAA (CYP11B1) NP_000488.3:n.1121+76_1121+78delinsGAA
NM_001026213.1:c.1121+76_1121+78delinsGAA (CYP11B1) NP_001021384.1:n.1121+76_1121+78delinsGAA...
XM_011516870.1:c.1199+76_1199+78delinsGAA (CYP11B1) XP_011515172.1:n.1199+76_1199+78delinsGAA...
XM_011516871.1:c.1199+76_1199+78delinsGAA (CYP11B1) XP_011515173.1:n.1199+76_1199+78delinsGAA...
XM_011516872.1:c.1121+76_1121+78delinsGAA (CYP11B1) XP_011515174.1:n.1121+76_1121+78delinsGAA...
XM_011516873.1:c.1199+76_1199+78delinsGAA (CYP11B1) XP_011515175.1:n.1199+76_1199+78delinsGAA...
XM_011516874.1:c.1199+76_1199+78delinsGAA (CYP11B1) XP_011515176.1:n.1199+76_1199+78delinsGAA...
XM_011516875.1:c.938+76_938+78delinsGAA (CYP11B1) XP_011515177.1:n.938+76_938+78delinsGAA
XM_011516876.1:c.1199+76_1199+78delinsGAA (CYP11B1) XP_011515178.1:n.1199+76_1199+78delinsGAA...
XM_011516970.1:c.214+34409_214+34411delinsTTC (GML) XP_011515272.1:n.214+34409_214+34411delin...
NM_000497.4:c.1121+76_1121+78delinsGAA (CYP11B1) MANE Select NP_000488.3:n.1121+76_1121+78delinsGAA