Canonical Allele Identifier: CA2269950073

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497341C= , CM000679.2:g.63497341C=	GRCh38
NC_000017.10:g.61574702C= , CM000679.1:g.61574702C=	GRCh37
NC_000017.9:g.58928434C=	NCBI36
NG_011648.1:g.25269C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3896C= MANE Select	ENSP00000290866.4:p.Ser1299=
ENST00000290863.10:c.2174C=	ENSP00000290863.6:p.Ser725=
ENST00000290866.9:c.3896C=	ENSP00000290866.4:p.Ser1299=
ENST00000413513.7:c.2051C=	ENSP00000392247.3:p.Ser684=
ENST00000428043.5:c.*318C=	ENSP00000397593.2:n.*318C=
ENST00000577647.2:c.1969+356C=	ENSP00000464149.1:n.1969+356C=
ENST00000578839.5:c.*1651C=	ENSP00000462110.2:n.*1651C=
ENST00000579314.5:c.*1625C=	ENSP00000462599.1:n.*1625C=
NM_000789.3:c.3896C=	NP_000780.1:p.Ser1299=
NM_001178057.1:c.2051C=	NP_001171528.1:p.Ser684=
NM_152830.2:c.2174C=	NP_690043.1:p.Ser725=
XM_005257110.1:c.3347C=	XP_005257167.1:p.Ser1116=
XM_006721737.2:c.2234C=	XP_006721800.2:p.Ser745=
XM_006721737.3:c.2234C=	XP_006721800.2:p.Ser745=
NM_000789.4:c.3896C= MANE Select	NP_000780.1:p.Ser1299=
NM_001178057.2:c.2051C=	NP_001171528.1:p.Ser684=
NM_152830.3:c.2174C=	NP_690043.1:p.Ser725=
NM_001382700.1:c.3329C=	NP_001369629.1:p.Ser1110=
NM_001382701.1:c.3044C=	NP_001369630.1:p.Ser1015=
NM_001382702.1:c.1511C=	NP_001369631.1:p.Ser504=
NR_168483.1:n.2274C=