Canonical Allele Identifier: CA1825496504

Gene: CYP11B1 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142875628_142875666delinsCCCAGATTCTGTCTGCCACCACCCAGTGGGGGCTGCTCT , CM000670.2:g.142875628_142875666delinsCCCAGATTCTGTCTGCCACCACCCAGTGGGGGCTGCTCT	GRCh38
NC_000008.10:g.143957044_143957082delinsCCCAGATTCTGTCTGCCACCACCCAGTGGGGGCTGCTCT , CM000670.1:g.143957044_143957082delinsCCCAGATTCTGTCTGCCACCACCCAGTGGGGGCTGCTCT	GRCh37
NC_000008.9:g.143954046_143954084delinsCCCAGATTCTGTCTGCCACCACCCAGTGGGGGCTGCTCT	NCBI36
NG_007954.1:g.9155_9193delinsAGAGCAGCCCCCACTGGGTGGTGGCAGACAGAATCTGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000292427.10:c.1121+46_1121+84delinsAGAGCAGCCCCCACTGGGTGGTGGCAGACAGAATCTGGG (CYP11B1) MANE Select	ENSP00000292427.5:n.1121+46_1121+84delins...
ENST00000292427.8:c.1121+46_1121+84delinsAGAGCAGCCCCCACTGGGTGGTGGCAGACAGAATCTGGG (CYP11B1)	ENSP00000292427.4:n.1121+46_1121+84delins...
ENST00000314111.4:n.1516+46_1516+84delinsAGAGCAGCCCCCACTGGGTGGTGGCAGACAGAATCTGGG (CYP11B1)
ENST00000377675.3:c.1334+46_1334+84delinsAGAGCAGCCCCCACTGGGTGGTGGCAGACAGAATCTGGG (CYP11B1)	ENSP00000366903.3:n.1334+46_1334+84delins...
ENST00000517471.5:c.1121+46_1121+84delinsAGAGCAGCCCCCACTGGGTGGTGGCAGACAGAATCTGGG (CYP11B1)	ENSP00000428043.1:n.1121+46_1121+84delins...
ENST00000519285.5:c.86+46_86+84delinsAGAGCAGCCCCCACTGGGTGGTGGCAGACAGAATCTGGG (CYP11B1)	ENSP00000430144.1:n.86+46_86+84delinsAGAG...
ENST00000522728.5:c.181+34403_181+34441delinsCCCAGATTCTGTCTGCCACCACCCAGTGGGGGCTGCTCT (GML)	ENSP00000430799.1:n.181+34403_181+34441de...
NM_000497.3:c.1121+46_1121+84delinsAGAGCAGCCCCCACTGGGTGGTGGCAGACAGAATCTGGG (CYP11B1)	NP_000488.3:n.1121+46_1121+84delinsAGAGCA...
NM_001026213.1:c.1121+46_1121+84delinsAGAGCAGCCCCCACTGGGTGGTGGCAGACAGAATCTGGG (CYP11B1)	NP_001021384.1:n.1121+46_1121+84delinsAGA...
XM_011516870.1:c.1199+46_1199+84delinsAGAGCAGCCCCCACTGGGTGGTGGCAGACAGAATCTGGG (CYP11B1)	XP_011515172.1:n.1199+46_1199+84delinsAGA...
XM_011516871.1:c.1199+46_1199+84delinsAGAGCAGCCCCCACTGGGTGGTGGCAGACAGAATCTGGG (CYP11B1)	XP_011515173.1:n.1199+46_1199+84delinsAGA...
XM_011516872.1:c.1121+46_1121+84delinsAGAGCAGCCCCCACTGGGTGGTGGCAGACAGAATCTGGG (CYP11B1)	XP_011515174.1:n.1121+46_1121+84delinsAGA...
XM_011516873.1:c.1199+46_1199+84delinsAGAGCAGCCCCCACTGGGTGGTGGCAGACAGAATCTGGG (CYP11B1)	XP_011515175.1:n.1199+46_1199+84delinsAGA...
XM_011516874.1:c.1199+46_1199+84delinsAGAGCAGCCCCCACTGGGTGGTGGCAGACAGAATCTGGG (CYP11B1)	XP_011515176.1:n.1199+46_1199+84delinsAGA...
XM_011516875.1:c.938+46_938+84delinsAGAGCAGCCCCCACTGGGTGGTGGCAGACAGAATCTGGG (CYP11B1)	XP_011515177.1:n.938+46_938+84delinsAGAGC...
XM_011516876.1:c.1199+46_1199+84delinsAGAGCAGCCCCCACTGGGTGGTGGCAGACAGAATCTGGG (CYP11B1)	XP_011515178.1:n.1199+46_1199+84delinsAGA...
XM_011516970.1:c.214+34403_214+34441delinsCCCAGATTCTGTCTGCCACCACCCAGTGGGGGCTGCTCT (GML)	XP_011515272.1:n.214+34403_214+34441delin...
NM_000497.4:c.1121+46_1121+84delinsAGAGCAGCCCCCACTGGGTGGTGGCAGACAGAATCTGGG (CYP11B1) MANE Select	NP_000488.3:n.1121+46_1121+84delinsAGAGCA...