Canonical Allele Identifier: CA8700572
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs766053859

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63496925G>A , CM000679.2:g.63496925G>A GRCh38
NC_000017.10:g.61574286G>A , CM000679.1:g.61574286G>A GRCh37
NC_000017.9:g.58928018G>A NCBI36
NG_011648.1:g.24853G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.3631G>A MANE Select ENSP00000290866.4:p.Glu1211Lys
ENST00000290863.10:c.1909G>A ENSP00000290863.6:p.Glu637Lys
ENST00000290866.9:c.3631G>A ENSP00000290866.4:p.Glu1211Lys
ENST00000413513.7:c.1786G>A ENSP00000392247.3:p.Glu596Lys
ENST00000428043.5:c.3631G>A ENSP00000397593.2:p.Glu1211Lys
ENST00000577418.5:n.641G>A
ENST00000577647.2:c.1909G>A ENSP00000464149.1:p.Glu637Lys
ENST00000578839.5:c.*1386G>A ENSP00000462110.2:n.*1386G>A
ENST00000579314.5:c.*1360G>A ENSP00000462599.1:n.*1360G>A
ENST00000579409.1:c.318G>A
ENST00000582244.1:n.505G>A
NM_000789.3:c.3631G>A NP_000780.1:p.Glu1211Lys
NM_001178057.1:c.1786G>A NP_001171528.1:p.Glu596Lys
NM_152830.2:c.1909G>A NP_690043.1:p.Glu637Lys
XM_005257110.1:c.3082G>A XP_005257167.1:p.Glu1028Lys
XM_006721737.2:c.1969G>A XP_006721800.2:p.Glu657Lys
XM_006721737.3:c.1969G>A XP_006721800.2:p.Glu657Lys
NM_000789.4:c.3631G>A MANE Select NP_000780.1:p.Glu1211Lys
NM_001178057.2:c.1786G>A NP_001171528.1:p.Glu596Lys
NM_152830.3:c.1909G>A NP_690043.1:p.Glu637Lys
NM_001382700.1:c.3064G>A NP_001369629.1:p.Glu1022Lys
NM_001382701.1:c.2779G>A NP_001369630.1:p.Glu927Lys
NM_001382702.1:c.1246G>A NP_001369631.1:p.Glu416Lys
NR_168483.1:n.2009G>A