Canonical Allele Identifier: CA2269944849

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486613G= , CM000679.2:g.63486613G=	GRCh38
NC_000017.10:g.61563974G= , CM000679.1:g.61563974G=	GRCh37
NC_000017.9:g.58917706G=	NCBI36
NG_011648.1:g.14541G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2115G= MANE Select	ENSP00000290866.4:p.Arg705=
ENST00000290863.10:c.393G=	ENSP00000290863.6:p.Arg131=
ENST00000290866.9:c.2115G=	ENSP00000290866.4:p.Arg705=
ENST00000413513.7:c.393G=	ENSP00000392247.3:p.Arg131=
ENST00000428043.5:c.2115G=	ENSP00000397593.2:p.Arg705=
ENST00000577647.2:c.393G=	ENSP00000464149.1:p.Arg131=
ENST00000578839.5:c.*185G=	ENSP00000462110.2:n.*185G=
ENST00000579204.1:c.296G=	ENSP00000464629.1:n.296G=
ENST00000579314.5:c.393G=	ENSP00000462599.1:p.Arg131=
ENST00000579726.5:c.677G=
ENST00000582005.5:c.*35G=	ENSP00000462002.1:n.*35G=
NM_000789.3:c.2115G=	NP_000780.1:p.Arg705=
NM_001178057.1:c.393G=	NP_001171528.1:p.Arg131=
NM_152830.2:c.393G=	NP_690043.1:p.Arg131=
XM_005257110.1:c.1566G=	XP_005257167.1:p.Arg522=
XM_006721737.2:c.453G=	XP_006721800.2:p.Arg151=
XM_006721737.3:c.453G=	XP_006721800.2:p.Arg151=
NM_000789.4:c.2115G= MANE Select	NP_000780.1:p.Arg705=
NM_001178057.2:c.393G=	NP_001171528.1:p.Arg131=
NM_152830.3:c.393G=	NP_690043.1:p.Arg131=
NM_001382700.1:c.1548G=	NP_001369629.1:p.Arg516=
NM_001382701.1:c.1263G=	NP_001369630.1:p.Arg421=
NM_001382702.1:c.45G=	NP_001369631.1:p.Arg15=
NR_168483.1:n.415G=