Canonical Allele Identifier: CA2269945067

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63487013A= , CM000679.2:g.63487013A=	GRCh38
NC_000017.10:g.61564374A= , CM000679.1:g.61564374A=	GRCh37
NC_000017.9:g.58918106A=	NCBI36
NG_011648.1:g.14941A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2245A= MANE Select	ENSP00000290866.4:p.Thr749=
ENST00000290863.10:c.523A=	ENSP00000290863.6:p.Thr175=
ENST00000290866.9:c.2245A=	ENSP00000290866.4:p.Thr749=
ENST00000413513.7:c.523A=	ENSP00000392247.3:p.Thr175=
ENST00000428043.5:c.2245A=	ENSP00000397593.2:p.Thr749=
ENST00000577647.2:c.523A=	ENSP00000464149.1:p.Thr175=
ENST00000578839.5:c.*315A=	ENSP00000462110.2:n.*315A=
ENST00000579204.1:c.426A=	ENSP00000464629.1:n.426A=
ENST00000579314.5:c.523A=	ENSP00000462599.1:p.Thr175=
ENST00000579726.5:c.807A=
ENST00000582005.5:c.*165A=	ENSP00000462002.1:n.*165A=
ENST00000582761.1:c.13A=	ENSP00000462909.1:p.Thr5=
ENST00000584865.5:n.191A=
NM_000789.3:c.2245A=	NP_000780.1:p.Thr749=
NM_001178057.1:c.523A=	NP_001171528.1:p.Thr175=
NM_152830.2:c.523A=	NP_690043.1:p.Thr175=
XM_005257110.1:c.1696A=	XP_005257167.1:p.Thr566=
XM_006721737.2:c.583A=	XP_006721800.2:p.Thr195=
XM_006721737.3:c.583A=	XP_006721800.2:p.Thr195=
NM_000789.4:c.2245A= MANE Select	NP_000780.1:p.Thr749=
NM_001178057.2:c.523A=	NP_001171528.1:p.Thr175=
NM_152830.3:c.523A=	NP_690043.1:p.Thr175=
NM_001382700.1:c.1678A=	NP_001369629.1:p.Thr560=
NM_001382701.1:c.1393A=	NP_001369630.1:p.Thr465=
NM_001382702.1:c.175A=	NP_001369631.1:p.Thr59=
NR_168483.1:n.545A=