Canonical Allele Identifier: CA2269942974

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63483172C= , CM000679.2:g.63483172C=	GRCh38
NC_000017.10:g.61560533C= , CM000679.1:g.61560533C=	GRCh37
NC_000017.9:g.58914265C=	NCBI36
NG_011648.1:g.11100C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000789.4:c.1486C= MANE Select	NP_000780.1:p.Arg496=
ENST00000290866.10:c.1486C= MANE Select	ENSP00000290866.4:p.Arg496=
NM_000789.3:c.1486C=	NP_000780.1:p.Arg496=
NM_001382700.1:c.919C=	NP_001369629.1:p.Arg307=
NM_001382701.1:c.634C=	NP_001369630.1:p.Arg212=
ENST00000290866.9:c.1486C=	ENSP00000290866.4:p.Arg496=
ENST00000428043.5:c.1486C=	ENSP00000397593.2:p.Arg496=
ENST00000582678.5:c.*885C=	ENSP00000462995.1:n.*885C=
ENST00000584529.5:n.1377-288C=
XM_005257110.1:c.937C=	XP_005257167.1:p.Arg313=