Canonical Allele Identifier: CA2269950055

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497316_63497319delinsCACT , CM000679.2:g.63497316_63497319delinsCACT	GRCh38
NC_000017.10:g.61574677_61574680delinsCACT , CM000679.1:g.61574677_61574680delinsCACT	GRCh37
NC_000017.9:g.58928409_58928412delinsCACT	NCBI36
NG_011648.1:g.25244_25247delinsCACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3871_3874delinsCACT MANE Select	ENSP00000290866.4:p.His1291=
ENST00000290863.10:c.2149_2152delinsCACT	ENSP00000290863.6:p.His717=
ENST00000290866.9:c.3871_3874delinsCACT	ENSP00000290866.4:p.His1291=
ENST00000413513.7:c.2026_2029delinsCACT	ENSP00000392247.3:p.His676=
ENST00000428043.5:c.*293_*296delinsCACT	ENSP00000397593.2:n.*293_*296delinsCACT
ENST00000577647.2:c.1969+331_1969+334delinsCACT	ENSP00000464149.1:n.1969+331_1969+334delinsCACT
ENST00000578839.5:c.*1626_*1629delinsCACT	ENSP00000462110.2:n.*1626_*1629delinsCACT
ENST00000579314.5:c.*1600_*1603delinsCACT	ENSP00000462599.1:n.*1600_*1603delinsCACT
NM_000789.3:c.3871_3874delinsCACT	NP_000780.1:p.His1291=
NM_001178057.1:c.2026_2029delinsCACT	NP_001171528.1:p.His676=
NM_152830.2:c.2149_2152delinsCACT	NP_690043.1:p.His717=
XM_005257110.1:c.3322_3325delinsCACT	XP_005257167.1:p.His1108=
XM_006721737.2:c.2209_2212delinsCACT	XP_006721800.2:p.His737=
XM_006721737.3:c.2209_2212delinsCACT	XP_006721800.2:p.His737=
NM_000789.4:c.3871_3874delinsCACT MANE Select	NP_000780.1:p.His1291=
NM_001178057.2:c.2026_2029delinsCACT	NP_001171528.1:p.His676=
NM_152830.3:c.2149_2152delinsCACT	NP_690043.1:p.His717=
NM_001382700.1:c.3304_3307delinsCACT	NP_001369629.1:p.His1102=
NM_001382701.1:c.3019_3022delinsCACT	NP_001369630.1:p.His1007=
NM_001382702.1:c.1486_1489delinsCACT	NP_001369631.1:p.His496=
NR_168483.1:n.2249_2252delinsCACT