Canonical Allele Identifier: CA2269949993

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497189G= , CM000679.2:g.63497189G=	GRCh38
NC_000017.10:g.61574550G= , CM000679.1:g.61574550G=	GRCh37
NC_000017.9:g.58928282G=	NCBI36
NG_011648.1:g.25117G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3744G= MANE Select	ENSP00000290866.4:p.Leu1248=
ENST00000290863.10:c.2022G=	ENSP00000290863.6:p.Leu674=
ENST00000290866.9:c.3744G=	ENSP00000290866.4:p.Leu1248=
ENST00000413513.7:c.1899G=	ENSP00000392247.3:p.Leu633=
ENST00000428043.5:c.*166G=	ENSP00000397593.2:n.*166G=
ENST00000577647.2:c.1969+204G=	ENSP00000464149.1:n.1969+204G=
ENST00000578839.5:c.*1499G=	ENSP00000462110.2:n.*1499G=
ENST00000579314.5:c.*1473G=	ENSP00000462599.1:n.*1473G=
NM_000789.3:c.3744G=	NP_000780.1:p.Leu1248=
NM_001178057.1:c.1899G=	NP_001171528.1:p.Leu633=
NM_152830.2:c.2022G=	NP_690043.1:p.Leu674=
XM_005257110.1:c.3195G=	XP_005257167.1:p.Leu1065=
XM_006721737.2:c.2082G=	XP_006721800.2:p.Leu694=
XM_006721737.3:c.2082G=	XP_006721800.2:p.Leu694=
NM_000789.4:c.3744G= MANE Select	NP_000780.1:p.Leu1248=
NM_001178057.2:c.1899G=	NP_001171528.1:p.Leu633=
NM_152830.3:c.2022G=	NP_690043.1:p.Leu674=
NM_001382700.1:c.3177G=	NP_001369629.1:p.Leu1059=
NM_001382701.1:c.2892G=	NP_001369630.1:p.Leu964=
NM_001382702.1:c.1359G=	NP_001369631.1:p.Leu453=
NR_168483.1:n.2122G=