Canonical Allele Identifier: CA2269949987

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497176G= , CM000679.2:g.63497176G=	GRCh38
NC_000017.10:g.61574537G= , CM000679.1:g.61574537G=	GRCh37
NC_000017.9:g.58928269G=	NCBI36
NG_011648.1:g.25104G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3731G= MANE Select	ENSP00000290866.4:p.Ser1244=
ENST00000290863.10:c.2009G=	ENSP00000290863.6:p.Ser670=
ENST00000290866.9:c.3731G=	ENSP00000290866.4:p.Ser1244=
ENST00000413513.7:c.1886G=	ENSP00000392247.3:p.Ser629=
ENST00000428043.5:c.*153G=	ENSP00000397593.2:n.*153G=
ENST00000577647.2:c.1969+191G=	ENSP00000464149.1:n.1969+191G=
ENST00000578839.5:c.*1486G=	ENSP00000462110.2:n.*1486G=
ENST00000579314.5:c.*1460G=	ENSP00000462599.1:n.*1460G=
NM_000789.3:c.3731G=	NP_000780.1:p.Ser1244=
NM_001178057.1:c.1886G=	NP_001171528.1:p.Ser629=
NM_152830.2:c.2009G=	NP_690043.1:p.Ser670=
XM_005257110.1:c.3182G=	XP_005257167.1:p.Ser1061=
XM_006721737.2:c.2069G=	XP_006721800.2:p.Ser690=
XM_006721737.3:c.2069G=	XP_006721800.2:p.Ser690=
NM_000789.4:c.3731G= MANE Select	NP_000780.1:p.Ser1244=
NM_001178057.2:c.1886G=	NP_001171528.1:p.Ser629=
NM_152830.3:c.2009G=	NP_690043.1:p.Ser670=
NM_001382700.1:c.3164G=	NP_001369629.1:p.Ser1055=
NM_001382701.1:c.2879G=	NP_001369630.1:p.Ser960=
NM_001382702.1:c.1346G=	NP_001369631.1:p.Ser449=
NR_168483.1:n.2109G=