Canonical Allele Identifier: CA8700532
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs753498859

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63496781G>A , CM000679.2:g.63496781G>A GRCh38
NC_000017.10:g.61574142G>A , CM000679.1:g.61574142G>A GRCh37
NC_000017.9:g.58927874G>A NCBI36
NG_011648.1:g.24709G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.3504-17G>A MANE Select ENSP00000290866.4:n.3504-17G>A
ENST00000290863.10:c.1782-17G>A ENSP00000290863.6:n.1782-17G>A
ENST00000290866.9:c.3504-17G>A ENSP00000290866.4:n.3504-17G>A
ENST00000413513.7:c.1659-17G>A ENSP00000392247.3:n.1659-17G>A
ENST00000428043.5:c.3504-17G>A ENSP00000397593.2:n.3504-17G>A
ENST00000577418.5:n.514-17G>A
ENST00000577647.2:c.1782-17G>A ENSP00000464149.1:n.1782-17G>A
ENST00000578839.5:c.*1259-17G>A ENSP00000462110.2:n.*1259-17G>A
ENST00000579314.5:c.*1233-17G>A ENSP00000462599.1:n.*1233-17G>A
ENST00000579409.1:c.191-17G>A
ENST00000582244.1:n.378-17G>A
NM_000789.3:c.3504-17G>A NP_000780.1:n.3504-17G>A
NM_001178057.1:c.1659-17G>A NP_001171528.1:n.1659-17G>A
NM_152830.2:c.1782-17G>A NP_690043.1:n.1782-17G>A
XM_005257110.1:c.2955-17G>A XP_005257167.1:n.2955-17G>A
XM_006721737.2:c.1842-17G>A XP_006721800.2:n.1842-17G>A
XM_006721737.3:c.1842-17G>A XP_006721800.2:n.1842-17G>A
NM_000789.4:c.3504-17G>A MANE Select NP_000780.1:n.3504-17G>A
NM_001178057.2:c.1659-17G>A NP_001171528.1:n.1659-17G>A
NM_152830.3:c.1782-17G>A NP_690043.1:n.1782-17G>A
NM_001382700.1:c.2937-17G>A NP_001369629.1:n.2937-17G>A
NM_001382701.1:c.2652-17G>A NP_001369630.1:n.2652-17G>A
NM_001382702.1:c.1119-17G>A NP_001369631.1:n.1119-17G>A
NR_168483.1:n.1882-17G>A