Canonical Allele Identifier: CA2269949781

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496863C= , CM000679.2:g.63496863C=	GRCh38
NC_000017.10:g.61574224C= , CM000679.1:g.61574224C=	GRCh37
NC_000017.9:g.58927956C=	NCBI36
NG_011648.1:g.24791C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3569C= MANE Select	ENSP00000290866.4:p.Pro1190=
ENST00000290863.10:c.1847C=	ENSP00000290863.6:p.Pro616=
ENST00000290866.9:c.3569C=	ENSP00000290866.4:p.Pro1190=
ENST00000413513.7:c.1724C=	ENSP00000392247.3:p.Pro575=
ENST00000428043.5:c.3569C=	ENSP00000397593.2:p.Pro1190=
ENST00000577418.5:n.579C=
ENST00000577647.2:c.1847C=	ENSP00000464149.1:p.Pro616=
ENST00000578839.5:c.*1324C=	ENSP00000462110.2:n.*1324C=
ENST00000579314.5:c.*1298C=	ENSP00000462599.1:n.*1298C=
ENST00000579409.1:c.256C=
ENST00000582244.1:n.443C=
NM_000789.3:c.3569C=	NP_000780.1:p.Pro1190=
NM_001178057.1:c.1724C=	NP_001171528.1:p.Pro575=
NM_152830.2:c.1847C=	NP_690043.1:p.Pro616=
XM_005257110.1:c.3020C=	XP_005257167.1:p.Pro1007=
XM_006721737.2:c.1907C=	XP_006721800.2:p.Pro636=
XM_006721737.3:c.1907C=	XP_006721800.2:p.Pro636=
NM_000789.4:c.3569C= MANE Select	NP_000780.1:p.Pro1190=
NM_001178057.2:c.1724C=	NP_001171528.1:p.Pro575=
NM_152830.3:c.1847C=	NP_690043.1:p.Pro616=
NM_001382700.1:c.3002C=	NP_001369629.1:p.Pro1001=
NM_001382701.1:c.2717C=	NP_001369630.1:p.Pro906=
NM_001382702.1:c.1184C=	NP_001369631.1:p.Pro395=
NR_168483.1:n.1947C=