Canonical Allele Identifier: CA2269949986

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497172G= , CM000679.2:g.63497172G=	GRCh38
NC_000017.10:g.61574533G= , CM000679.1:g.61574533G=	GRCh37
NC_000017.9:g.58928265G=	NCBI36
NG_011648.1:g.25100G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3727G= MANE Select	ENSP00000290866.4:p.Val1243=
ENST00000290863.10:c.2005G=	ENSP00000290863.6:p.Val669=
ENST00000290866.9:c.3727G=	ENSP00000290866.4:p.Val1243=
ENST00000413513.7:c.1882G=	ENSP00000392247.3:p.Val628=
ENST00000428043.5:c.*149G=	ENSP00000397593.2:n.*149G=
ENST00000577647.2:c.1969+187G=	ENSP00000464149.1:n.1969+187G=
ENST00000578839.5:c.*1482G=	ENSP00000462110.2:n.*1482G=
ENST00000579314.5:c.*1456G=	ENSP00000462599.1:n.*1456G=
NM_000789.3:c.3727G=	NP_000780.1:p.Val1243=
NM_001178057.1:c.1882G=	NP_001171528.1:p.Val628=
NM_152830.2:c.2005G=	NP_690043.1:p.Val669=
XM_005257110.1:c.3178G=	XP_005257167.1:p.Val1060=
XM_006721737.2:c.2065G=	XP_006721800.2:p.Val689=
XM_006721737.3:c.2065G=	XP_006721800.2:p.Val689=
NM_000789.4:c.3727G= MANE Select	NP_000780.1:p.Val1243=
NM_001178057.2:c.1882G=	NP_001171528.1:p.Val628=
NM_152830.3:c.2005G=	NP_690043.1:p.Val669=
NM_001382700.1:c.3160G=	NP_001369629.1:p.Val1054=
NM_001382701.1:c.2875G=	NP_001369630.1:p.Val959=
NM_001382702.1:c.1342G=	NP_001369631.1:p.Val448=
NR_168483.1:n.2105G=