Canonical Allele Identifier: CA2269949764

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496828G= , CM000679.2:g.63496828G=	GRCh38
NC_000017.10:g.61574189G= , CM000679.1:g.61574189G=	GRCh37
NC_000017.9:g.58927921G=	NCBI36
NG_011648.1:g.24756G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3534G= MANE Select	ENSP00000290866.4:p.Pro1178=
ENST00000290863.10:c.1812G=	ENSP00000290863.6:p.Pro604=
ENST00000290866.9:c.3534G=	ENSP00000290866.4:p.Pro1178=
ENST00000413513.7:c.1689G=	ENSP00000392247.3:p.Pro563=
ENST00000428043.5:c.3534G=	ENSP00000397593.2:p.Pro1178=
ENST00000577418.5:n.544G=
ENST00000577647.2:c.1812G=	ENSP00000464149.1:p.Pro604=
ENST00000578839.5:c.*1289G=	ENSP00000462110.2:n.*1289G=
ENST00000579314.5:c.*1263G=	ENSP00000462599.1:n.*1263G=
ENST00000579409.1:c.221G=
ENST00000582244.1:n.408G=
NM_000789.3:c.3534G=	NP_000780.1:p.Pro1178=
NM_001178057.1:c.1689G=	NP_001171528.1:p.Pro563=
NM_152830.2:c.1812G=	NP_690043.1:p.Pro604=
XM_005257110.1:c.2985G=	XP_005257167.1:p.Pro995=
XM_006721737.2:c.1872G=	XP_006721800.2:p.Pro624=
XM_006721737.3:c.1872G=	XP_006721800.2:p.Pro624=
NM_000789.4:c.3534G= MANE Select	NP_000780.1:p.Pro1178=
NM_001178057.2:c.1689G=	NP_001171528.1:p.Pro563=
NM_152830.3:c.1812G=	NP_690043.1:p.Pro604=
NM_001382700.1:c.2967G=	NP_001369629.1:p.Pro989=
NM_001382701.1:c.2682G=	NP_001369630.1:p.Pro894=
NM_001382702.1:c.1149G=	NP_001369631.1:p.Pro383=
NR_168483.1:n.1912G=