Canonical Allele Identifier: CA2269940250

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477990G= , CM000679.2:g.63477990G=	GRCh38
NC_000017.10:g.61555351G= , CM000679.1:g.61555351G=	GRCh37
NC_000017.9:g.58909083G=	NCBI36
NG_011648.1:g.5918G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.309G= MANE Select	ENSP00000290866.4:p.Glu103=
ENST00000290866.9:c.309G=	ENSP00000290866.4:p.Glu103=
ENST00000428043.5:c.309G=	ENSP00000397593.2:p.Glu103=
ENST00000579462.1:n.334G=
ENST00000580318.1:n.498G=
ENST00000582627.1:c.309G=	ENSP00000462280.1:p.Glu103=
ENST00000582678.5:c.309G=	ENSP00000462995.1:p.Glu103=
ENST00000583336.5:n.343G=
ENST00000584529.5:n.343G=
NM_000789.3:c.309G=	NP_000780.1:p.Glu103=
XM_005257110.1:c.-147G=	XP_005257167.1:n.-147G=
NM_000789.4:c.309G= MANE Select	NP_000780.1:p.Glu103=
NM_001382700.1:c.74G=	NP_001369629.1:p.Ser25=
NM_001382701.1:c.-306G=	NP_001369630.1:n.-306G=