Canonical Allele Identifier: CA2969559221

Gene: CYP11B1 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142876156_142876158del , CM000670.2:g.142876156_142876158del	GRCh38
NC_000008.10:g.143957572_143957574del , CM000670.1:g.143957572_143957574del	GRCh37
NC_000008.9:g.143954574_143954576del	NCBI36
NG_007954.1:g.8664_8666del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.954+84_954+86del (CYP11B1) MANE Select	ENSP00000292427.5:n.954+84_954+86del
ENST00000292427.8:c.954+84_954+86del (CYP11B1)	ENSP00000292427.4:n.954+84_954+86del
ENST00000314111.4:n.1071_1073del (CYP11B1)
ENST00000377675.3:c.1167+84_1167+86del (CYP11B1)	ENSP00000366903.3:n.1167+84_1167+86del
ENST00000517471.5:c.954+84_954+86del (CYP11B1)	ENSP00000428043.1:n.954+84_954+86del
ENST00000522728.5:c.181+34931_181+34933del (GML)	ENSP00000430799.1:n.181+34931_181+34933del
NM_000497.3:c.954+84_954+86del (CYP11B1)	NP_000488.3:n.954+84_954+86del
NM_001026213.1:c.954+84_954+86del (CYP11B1)	NP_001021384.1:n.954+84_954+86del
XM_011516870.1:c.1032+84_1032+86del (CYP11B1)	XP_011515172.1:n.1032+84_1032+86del
XM_011516871.1:c.1032+84_1032+86del (CYP11B1)	XP_011515173.1:n.1032+84_1032+86del
XM_011516872.1:c.954+84_954+86del (CYP11B1)	XP_011515174.1:n.954+84_954+86del
XM_011516873.1:c.1032+84_1032+86del (CYP11B1)	XP_011515175.1:n.1032+84_1032+86del
XM_011516874.1:c.1032+84_1032+86del (CYP11B1)	XP_011515176.1:n.1032+84_1032+86del
XM_011516875.1:c.771+84_771+86del (CYP11B1)	XP_011515177.1:n.771+84_771+86del
XM_011516876.1:c.1032+84_1032+86del (CYP11B1)	XP_011515178.1:n.1032+84_1032+86del
XM_011516970.1:c.214+34931_214+34933del (GML)	XP_011515272.1:n.214+34931_214+34933del
NM_000497.4:c.954+84_954+86del (CYP11B1) MANE Select	NP_000488.3:n.954+84_954+86del