Canonical Allele Identifier: CA8699950
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs769028657

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63486659A>G , CM000679.2:g.63486659A>G GRCh38
NC_000017.10:g.61564020A>G , CM000679.1:g.61564020A>G GRCh37
NC_000017.9:g.58917752A>G NCBI36
NG_011648.1:g.14587A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.2161A>G MANE Select ENSP00000290866.4:p.Ile721Val
ENST00000290863.10:c.439A>G ENSP00000290863.6:p.Ile147Val
ENST00000290866.9:c.2161A>G ENSP00000290866.4:p.Ile721Val
ENST00000413513.7:c.439A>G ENSP00000392247.3:p.Ile147Val
ENST00000428043.5:c.2161A>G ENSP00000397593.2:p.Ile721Val
ENST00000577647.2:c.439A>G ENSP00000464149.1:p.Ile147Val
ENST00000578839.5:c.*231A>G ENSP00000462110.2:n.*231A>G
ENST00000579204.1:c.342A>G ENSP00000464629.1:n.342A>G
ENST00000579314.5:c.439A>G ENSP00000462599.1:p.Ile147Val
ENST00000579726.5:c.723A>G
ENST00000582005.5:c.*81A>G ENSP00000462002.1:n.*81A>G
NM_000789.3:c.2161A>G NP_000780.1:p.Ile721Val
NM_001178057.1:c.439A>G NP_001171528.1:p.Ile147Val
NM_152830.2:c.439A>G NP_690043.1:p.Ile147Val
XM_005257110.1:c.1612A>G XP_005257167.1:p.Ile538Val
XM_006721737.2:c.499A>G XP_006721800.2:p.Ile167Val
XM_006721737.3:c.499A>G XP_006721800.2:p.Ile167Val
NM_000789.4:c.2161A>G MANE Select NP_000780.1:p.Ile721Val
NM_001178057.2:c.439A>G NP_001171528.1:p.Ile147Val
NM_152830.3:c.439A>G NP_690043.1:p.Ile147Val
NM_001382700.1:c.1594A>G NP_001369629.1:p.Ile532Val
NM_001382701.1:c.1309A>G NP_001369630.1:p.Ile437Val
NM_001382702.1:c.91A>G NP_001369631.1:p.Ile31Val
NR_168483.1:n.461A>G