Canonical Allele Identifier: CA2269940301

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63478090C= , CM000679.2:g.63478090C=	GRCh38
NC_000017.10:g.61555451C= , CM000679.1:g.61555451C=	GRCh37
NC_000017.9:g.58909183C=	NCBI36
NG_011648.1:g.6018C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.409C= MANE Select	ENSP00000290866.4:p.Arg137=
ENST00000290866.9:c.409C=	ENSP00000290866.4:p.Arg137=
ENST00000428043.5:c.409C=	ENSP00000397593.2:p.Arg137=
ENST00000579462.1:n.434C=
ENST00000580318.1:n.598C=
ENST00000582627.1:c.409C=	ENSP00000462280.1:p.Arg137=
ENST00000582678.5:c.409C=	ENSP00000462995.1:p.Arg137=
ENST00000583336.5:n.443C=
ENST00000584529.5:n.443C=
NM_000789.3:c.409C=	NP_000780.1:p.Arg137=
XM_005257110.1:c.-47C=	XP_005257167.1:n.-47C=
NM_000789.4:c.409C= MANE Select	NP_000780.1:p.Arg137=
NM_001382700.1:c.174C=	NP_001369629.1:p.Ser58=
NM_001382701.1:c.-206C=	NP_001369630.1:n.-206C=