Canonical Allele Identifier: CA2187638051

Gene: CYP11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74339752G= , CM000677.2:g.74339752G=	GRCh38
NC_000015.9:g.74632093G= , CM000677.1:g.74632093G=	GRCh37
NC_000015.8:g.72419146G=	NCBI36
NG_007973.1:g.32990C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268053.11:c.992C= MANE Select	ENSP00000268053.6:p.Thr331=
ENST00000268053.10:c.992C=	ENSP00000268053.6:p.Thr331=
ENST00000358632.8:c.518C=	ENSP00000351455.4:p.Thr173=
ENST00000435365.5:c.992C=	ENSP00000391081.1:p.Thr331=
ENST00000566674.5:c.518C=	ENSP00000456941.1:p.Thr173=
NM_000781.2:c.992C=	NP_000772.2:p.Thr331=
NM_001099773.1:c.518C=	NP_001093243.1:p.Thr173=
NM_000781.3:c.992C= MANE Select	NP_000772.2:p.Thr331=
NM_001099773.2:c.518C=	NP_001093243.1:p.Thr173=