Canonical Allele Identifier: CA2269950063

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497324C= , CM000679.2:g.63497324C=	GRCh38
NC_000017.10:g.61574685C= , CM000679.1:g.61574685C=	GRCh37
NC_000017.9:g.58928417C=	NCBI36
NG_011648.1:g.25252C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3879C= MANE Select	ENSP00000290866.4:p.His1293=
ENST00000290863.10:c.2157C=	ENSP00000290863.6:p.His719=
ENST00000290866.9:c.3879C=	ENSP00000290866.4:p.His1293=
ENST00000413513.7:c.2034C=	ENSP00000392247.3:p.His678=
ENST00000428043.5:c.*301C=	ENSP00000397593.2:n.*301C=
ENST00000577647.2:c.1969+339C=	ENSP00000464149.1:n.1969+339C=
ENST00000578839.5:c.*1634C=	ENSP00000462110.2:n.*1634C=
ENST00000579314.5:c.*1608C=	ENSP00000462599.1:n.*1608C=
NM_000789.3:c.3879C=	NP_000780.1:p.His1293=
NM_001178057.1:c.2034C=	NP_001171528.1:p.His678=
NM_152830.2:c.2157C=	NP_690043.1:p.His719=
XM_005257110.1:c.3330C=	XP_005257167.1:p.His1110=
XM_006721737.2:c.2217C=	XP_006721800.2:p.His739=
XM_006721737.3:c.2217C=	XP_006721800.2:p.His739=
NM_000789.4:c.3879C= MANE Select	NP_000780.1:p.His1293=
NM_001178057.2:c.2034C=	NP_001171528.1:p.His678=
NM_152830.3:c.2157C=	NP_690043.1:p.His719=
NM_001382700.1:c.3312C=	NP_001369629.1:p.His1104=
NM_001382701.1:c.3027C=	NP_001369630.1:p.His1009=
NM_001382702.1:c.1494C=	NP_001369631.1:p.His498=
NR_168483.1:n.2257C=