Canonical Allele Identifier: CA400567978
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63496992C>A , CM000679.2:g.63496992C>A GRCh38
NC_000017.10:g.61574353C>A , CM000679.1:g.61574353C>A GRCh37
NC_000017.9:g.58928085C>A NCBI36
NG_011648.1:g.24920C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.3691+7C>A MANE Select ENSP00000290866.4:n.3691+7C>A
ENST00000290863.10:c.1969+7C>A ENSP00000290863.6:n.1969+7C>A
ENST00000290866.9:c.3691+7C>A ENSP00000290866.4:n.3691+7C>A
ENST00000413513.7:c.1846+7C>A ENSP00000392247.3:n.1846+7C>A
ENST00000428043.5:c.3698C>A ENSP00000397593.2:p.Ala1233Asp
ENST00000577418.5:n.701+7C>A
ENST00000577647.2:c.1969+7C>A ENSP00000464149.1:n.1969+7C>A
ENST00000578839.5:c.*1446+7C>A ENSP00000462110.2:n.*1446+7C>A
ENST00000579314.5:c.*1420+7C>A ENSP00000462599.1:n.*1420+7C>A
ENST00000579409.1:c.385C>A
NM_000789.3:c.3691+7C>A NP_000780.1:n.3691+7C>A
NM_001178057.1:c.1846+7C>A NP_001171528.1:n.1846+7C>A
NM_152830.2:c.1969+7C>A NP_690043.1:n.1969+7C>A
XM_005257110.1:c.3142+7C>A XP_005257167.1:n.3142+7C>A
XM_006721737.2:c.2029+7C>A XP_006721800.2:n.2029+7C>A
XM_006721737.3:c.2029+7C>A XP_006721800.2:n.2029+7C>A
NM_000789.4:c.3691+7C>A MANE Select NP_000780.1:n.3691+7C>A
NM_001178057.2:c.1846+7C>A NP_001171528.1:n.1846+7C>A
NM_152830.3:c.1969+7C>A NP_690043.1:n.1969+7C>A
NM_001382700.1:c.3124+7C>A NP_001369629.1:n.3124+7C>A
NM_001382701.1:c.2839+7C>A NP_001369630.1:n.2839+7C>A
NM_001382702.1:c.1306+7C>A NP_001369631.1:n.1306+7C>A
NR_168483.1:n.2069+7C>A