Canonical Allele Identifier: CA2269950025

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497256G= , CM000679.2:g.63497256G=	GRCh38
NC_000017.10:g.61574617G= , CM000679.1:g.61574617G=	GRCh37
NC_000017.9:g.58928349G=	NCBI36
NG_011648.1:g.25184G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3811G= MANE Select	ENSP00000290866.4:p.Val1271=
ENST00000290863.10:c.2089G=	ENSP00000290863.6:p.Val697=
ENST00000290866.9:c.3811G=	ENSP00000290866.4:p.Val1271=
ENST00000413513.7:c.1966G=	ENSP00000392247.3:p.Val656=
ENST00000428043.5:c.*233G=	ENSP00000397593.2:n.*233G=
ENST00000577647.2:c.1969+271G=	ENSP00000464149.1:n.1969+271G=
ENST00000578839.5:c.*1566G=	ENSP00000462110.2:n.*1566G=
ENST00000579314.5:c.*1540G=	ENSP00000462599.1:n.*1540G=
NM_000789.3:c.3811G=	NP_000780.1:p.Val1271=
NM_001178057.1:c.1966G=	NP_001171528.1:p.Val656=
NM_152830.2:c.2089G=	NP_690043.1:p.Val697=
XM_005257110.1:c.3262G=	XP_005257167.1:p.Val1088=
XM_006721737.2:c.2149G=	XP_006721800.2:p.Val717=
XM_006721737.3:c.2149G=	XP_006721800.2:p.Val717=
NM_000789.4:c.3811G= MANE Select	NP_000780.1:p.Val1271=
NM_001178057.2:c.1966G=	NP_001171528.1:p.Val656=
NM_152830.3:c.2089G=	NP_690043.1:p.Val697=
NM_001382700.1:c.3244G=	NP_001369629.1:p.Val1082=
NM_001382701.1:c.2959G=	NP_001369630.1:p.Val987=
NM_001382702.1:c.1426G=	NP_001369631.1:p.Val476=
NR_168483.1:n.2189G=