Canonical Allele Identifier: CA372392342

Gene: CYP11B1 GML

Linked Data

• MyVariant Identifiers: chr8:g.143956678A>G (hg19) ; chr8:g.142875262A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142875262A>G , CM000670.2:g.142875262A>G	GRCh38
NC_000008.10:g.143956678A>G , CM000670.1:g.143956678A>G	GRCh37
NC_000008.9:g.143953680A>G	NCBI36
NG_007954.1:g.9559T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.1172T>C (CYP11B1) MANE Select	ENSP00000292427.5:p.Val391Ala
ENST00000292427.8:c.1172T>C (CYP11B1)	ENSP00000292427.4:p.Val391Ala
ENST00000314111.4:n.1567T>C (CYP11B1)
ENST00000377675.3:c.1385T>C (CYP11B1)	ENSP00000366903.3:p.Val462Ala
ENST00000517471.5:c.1172T>C (CYP11B1)	ENSP00000428043.1:p.Val391Ala
ENST00000519285.5:c.206T>C (CYP11B1)	ENSP00000430144.1:p.Val69Ala
ENST00000522728.5:c.181+34037A>G (GML)	ENSP00000430799.1:n.181+34037A>G
NM_000497.3:c.1172T>C (CYP11B1)	NP_000488.3:p.Val391Ala
NM_001026213.1:c.1172T>C (CYP11B1)	NP_001021384.1:p.Val391Ala
XM_011516870.1:c.1319T>C (CYP11B1)	XP_011515172.1:p.Val440Ala
XM_011516871.1:c.1250T>C (CYP11B1)	XP_011515173.1:p.Val417Ala
XM_011516872.1:c.1241T>C (CYP11B1)	XP_011515174.1:p.Val414Ala
XM_011516873.1:c.1319T>C (CYP11B1)	XP_011515175.1:p.Val440Ala
XM_011516874.1:c.1250T>C (CYP11B1)	XP_011515176.1:p.Val417Ala
XM_011516875.1:c.1058T>C (CYP11B1)	XP_011515177.1:p.Val353Ala
XM_011516876.1:c.1319T>C (CYP11B1)	XP_011515178.1:p.Val440Ala
XM_011516970.1:c.214+34037A>G (GML)	XP_011515272.1:n.214+34037A>G
NM_000497.4:c.1172T>C (CYP11B1) MANE Select	NP_000488.3:p.Val391Ala