Canonical Allele Identifier: CA1825495794

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142874445G= , CM000670.2:g.142874445G= GRCh38
NC_000008.10:g.143955861G= , CM000670.1:g.143955861G= GRCh37
NC_000008.9:g.143952863G= NCBI36
NG_007954.1:g.10376C=

Transcript Alleles

HGVS Amino-acid change
ENST00000292427.10:c.1440C= (CYP11B1) MANE Select ENSP00000292427.5:p.Asp480=
ENST00000292427.8:c.1440C= (CYP11B1) ENSP00000292427.4:p.Asp480=
ENST00000314111.4:n.1637C= (CYP11B1)
ENST00000377675.3:c.1653C= (CYP11B1) ENSP00000366903.3:p.Asp551=
ENST00000517471.5:c.1242C= (CYP11B1) ENSP00000428043.1:p.Asp414=
ENST00000519285.5:c.474C= (CYP11B1) ENSP00000430144.1:p.Asp158=
ENST00000522728.5:c.181+33220G= (GML) ENSP00000430799.1:n.181+33220G=
NM_000497.3:c.1440C= (CYP11B1) NP_000488.3:p.Asp480=
NM_001026213.1:c.1242C= (CYP11B1) NP_001021384.1:p.Asp414=
XM_011516870.1:c.1678C= (CYP11B1) XP_011515172.1:p.His560=
XM_011516871.1:c.1609C= (CYP11B1) XP_011515173.1:p.His537=
XM_011516872.1:c.1600C= (CYP11B1) XP_011515174.1:p.His534=
XM_011516873.1:c.1587C= (CYP11B1) XP_011515175.1:p.Asp529=
XM_011516874.1:c.1518C= (CYP11B1) XP_011515176.1:p.Asp506=
XM_011516875.1:c.1417C= (CYP11B1) XP_011515177.1:p.His473=
XM_011516876.1:c.1389C= (CYP11B1) XP_011515178.1:p.Asp463=
XM_011516970.1:c.214+33220G= (GML) XP_011515272.1:n.214+33220G=
NM_000497.4:c.1440C= (CYP11B1) MANE Select NP_000488.3:p.Asp480=