Canonical Allele Identifier: CA292884326
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs4344

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63489363G>C , CM000679.2:g.63489363G>C GRCh38
NC_000017.10:g.61566724G>C , CM000679.1:g.61566724G>C GRCh37
NC_000017.9:g.58920456G>C NCBI36
NG_011648.1:g.17291G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.2641+231G>C MANE Select ENSP00000290866.4:n.2641+231G>C
ENST00000290863.10:c.919+231G>C ENSP00000290863.6:n.919+231G>C
ENST00000290866.9:c.2641+231G>C ENSP00000290866.4:n.2641+231G>C
ENST00000413513.7:c.919+231G>C ENSP00000392247.3:n.919+231G>C
ENST00000428043.5:c.2641+231G>C ENSP00000397593.2:n.2641+231G>C
ENST00000577647.2:c.919+231G>C ENSP00000464149.1:n.919+231G>C
ENST00000578839.5:c.*519+572G>C ENSP00000462110.2:n.*519+572G>C
ENST00000579314.5:c.*370+231G>C ENSP00000462599.1:n.*370+231G>C
ENST00000582761.1:c.409+231G>C ENSP00000462909.1:n.409+231G>C
ENST00000584865.5:n.587+231G>C
NM_000789.3:c.2641+231G>C NP_000780.1:n.2641+231G>C
NM_001178057.1:c.919+231G>C NP_001171528.1:n.919+231G>C
NM_152830.2:c.919+231G>C NP_690043.1:n.919+231G>C
XM_005257110.1:c.2092+231G>C XP_005257167.1:n.2092+231G>C
XM_006721737.2:c.979+231G>C XP_006721800.2:n.979+231G>C
XM_006721737.3:c.979+231G>C XP_006721800.2:n.979+231G>C
NM_000789.4:c.2641+231G>C MANE Select NP_000780.1:n.2641+231G>C
NM_001178057.2:c.919+231G>C NP_001171528.1:n.919+231G>C
NM_152830.3:c.919+231G>C NP_690043.1:n.919+231G>C
NM_001382700.1:c.2074+231G>C NP_001369629.1:n.2074+231G>C
NM_001382701.1:c.1789+231G>C NP_001369630.1:n.1789+231G>C
NM_001382702.1:c.379+572G>C NP_001369631.1:n.379+572G>C
NR_168483.1:n.1019+231G>C