Canonical Allele Identifier: CA2269940258

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63478011G= , CM000679.2:g.63478011G=	GRCh38
NC_000017.10:g.61555372G= , CM000679.1:g.61555372G=	GRCh37
NC_000017.9:g.58909104G=	NCBI36
NG_011648.1:g.5939G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.330G= MANE Select	ENSP00000290866.4:p.Gln110=
ENST00000290866.9:c.330G=	ENSP00000290866.4:p.Gln110=
ENST00000428043.5:c.330G=	ENSP00000397593.2:p.Gln110=
ENST00000579462.1:n.355G=
ENST00000580318.1:n.519G=
ENST00000582627.1:c.330G=	ENSP00000462280.1:p.Gln110=
ENST00000582678.5:c.330G=	ENSP00000462995.1:p.Gln110=
ENST00000583336.5:n.364G=
ENST00000584529.5:n.364G=
NM_000789.3:c.330G=	NP_000780.1:p.Gln110=
XM_005257110.1:c.-126G=	XP_005257167.1:n.-126G=
NM_000789.4:c.330G= MANE Select	NP_000780.1:p.Gln110=
NM_001382700.1:c.95G=	NP_001369629.1:p.Arg32=
NM_001382701.1:c.-285G=	NP_001369630.1:n.-285G=