Canonical Allele Identifier: CA1825496867

Gene: CYP11B1 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142876165_142876166delinsTG , CM000670.2:g.142876165_142876166delinsTG	GRCh38
NC_000008.10:g.143957581_143957582delinsTG , CM000670.1:g.143957581_143957582delinsTG	GRCh37
NC_000008.9:g.143954583_143954584delinsTG	NCBI36
NG_007954.1:g.8655_8656delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000292427.10:c.954+75_954+76delinsCA (CYP11B1) MANE Select	ENSP00000292427.5:n.954+75_954+76delinsCA
ENST00000292427.8:c.954+75_954+76delinsCA (CYP11B1)	ENSP00000292427.4:n.954+75_954+76delinsCA
ENST00000314111.4:n.1062_1063delinsCA (CYP11B1)
ENST00000377675.3:c.1167+75_1167+76delinsCA (CYP11B1)	ENSP00000366903.3:n.1167+75_1167+76delinsCA
ENST00000517471.5:c.954+75_954+76delinsCA (CYP11B1)	ENSP00000428043.1:n.954+75_954+76delinsCA
ENST00000522728.5:c.181+34940_181+34941delinsTG (GML)	ENSP00000430799.1:n.181+34940_181+34941delinsTG
NM_000497.3:c.954+75_954+76delinsCA (CYP11B1)	NP_000488.3:n.954+75_954+76delinsCA
NM_001026213.1:c.954+75_954+76delinsCA (CYP11B1)	NP_001021384.1:n.954+75_954+76delinsCA
XM_011516870.1:c.1032+75_1032+76delinsCA (CYP11B1)	XP_011515172.1:n.1032+75_1032+76delinsCA
XM_011516871.1:c.1032+75_1032+76delinsCA (CYP11B1)	XP_011515173.1:n.1032+75_1032+76delinsCA
XM_011516872.1:c.954+75_954+76delinsCA (CYP11B1)	XP_011515174.1:n.954+75_954+76delinsCA
XM_011516873.1:c.1032+75_1032+76delinsCA (CYP11B1)	XP_011515175.1:n.1032+75_1032+76delinsCA
XM_011516874.1:c.1032+75_1032+76delinsCA (CYP11B1)	XP_011515176.1:n.1032+75_1032+76delinsCA
XM_011516875.1:c.771+75_771+76delinsCA (CYP11B1)	XP_011515177.1:n.771+75_771+76delinsCA
XM_011516876.1:c.1032+75_1032+76delinsCA (CYP11B1)	XP_011515178.1:n.1032+75_1032+76delinsCA
XM_011516970.1:c.214+34940_214+34941delinsTG (GML)	XP_011515272.1:n.214+34940_214+34941delinsTG
NM_000497.4:c.954+75_954+76delinsCA (CYP11B1) MANE Select	NP_000488.3:n.954+75_954+76delinsCA