Canonical Allele Identifier: CA2269942621

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63482525G= , CM000679.2:g.63482525G=	GRCh38
NC_000017.10:g.61559886G= , CM000679.1:g.61559886G=	GRCh37
NC_000017.9:g.58913618G=	NCBI36
NG_011648.1:g.10453G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.1178G= MANE Select	ENSP00000290866.4:p.Gly393=
ENST00000290866.9:c.1178G=	ENSP00000290866.4:p.Gly393=
ENST00000428043.5:c.1178G=	ENSP00000397593.2:p.Gly393=
ENST00000582678.5:c.*577G=	ENSP00000462995.1:n.*577G=
ENST00000584529.5:n.1212G=
NM_000789.3:c.1178G=	NP_000780.1:p.Gly393=
XM_005257110.1:c.629G=	XP_005257167.1:p.Gly210=
NM_000789.4:c.1178G= MANE Select	NP_000780.1:p.Gly393=
NM_001382700.1:c.611G=	NP_001369629.1:p.Gly204=
NM_001382701.1:c.326G=	NP_001369630.1:p.Gly109=