Canonical Allele Identifier: CA2269949821

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496939T= , CM000679.2:g.63496939T=	GRCh38
NC_000017.10:g.61574300T= , CM000679.1:g.61574300T=	GRCh37
NC_000017.9:g.58928032T=	NCBI36
NG_011648.1:g.24867T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3645T= MANE Select	ENSP00000290866.4:p.His1215=
ENST00000290863.10:c.1923T=	ENSP00000290863.6:p.His641=
ENST00000290866.9:c.3645T=	ENSP00000290866.4:p.His1215=
ENST00000413513.7:c.1800T=	ENSP00000392247.3:p.His600=
ENST00000428043.5:c.3645T=	ENSP00000397593.2:p.His1215=
ENST00000577418.5:n.655T=
ENST00000577647.2:c.1923T=	ENSP00000464149.1:p.His641=
ENST00000578839.5:c.*1400T=	ENSP00000462110.2:n.*1400T=
ENST00000579314.5:c.*1374T=	ENSP00000462599.1:n.*1374T=
ENST00000579409.1:c.332T=
ENST00000582244.1:n.519T=
NM_000789.3:c.3645T=	NP_000780.1:p.His1215=
NM_001178057.1:c.1800T=	NP_001171528.1:p.His600=
NM_152830.2:c.1923T=	NP_690043.1:p.His641=
XM_005257110.1:c.3096T=	XP_005257167.1:p.His1032=
XM_006721737.2:c.1983T=	XP_006721800.2:p.His661=
XM_006721737.3:c.1983T=	XP_006721800.2:p.His661=
NM_000789.4:c.3645T= MANE Select	NP_000780.1:p.His1215=
NM_001178057.2:c.1800T=	NP_001171528.1:p.His600=
NM_152830.3:c.1923T=	NP_690043.1:p.His641=
NM_001382700.1:c.3078T=	NP_001369629.1:p.His1026=
NM_001382701.1:c.2793T=	NP_001369630.1:p.His931=
NM_001382702.1:c.1260T=	NP_001369631.1:p.His420=
NR_168483.1:n.2023T=