Canonical Allele Identifier: CA2963774967
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63488682dup , CM000679.2:g.63488682dup GRCh38
NC_000017.10:g.61566043dup , CM000679.1:g.61566043dup GRCh37
NC_000017.9:g.58919775dup NCBI36
NG_011648.1:g.16610dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.2340dup MANE Select ENSP00000290866.4:p.Glu781Ter
ENST00000290863.10:c.618dup ENSP00000290863.6:p.Glu207Ter
ENST00000290866.9:c.2340dup ENSP00000290866.4:p.Glu781Ter
ENST00000413513.7:c.618dup ENSP00000392247.3:p.Glu207Ter
ENST00000428043.5:c.2340dup ENSP00000397593.2:p.Glu781Ter
ENST00000577647.2:c.618dup ENSP00000464149.1:p.Glu207Ter
ENST00000578839.5:c.*410dup ENSP00000462110.2:n.*410dup
ENST00000579204.1:c.599dup ENSP00000464629.1:n.599dup
ENST00000579314.5:c.*69dup ENSP00000462599.1:n.*69dup
ENST00000582005.5:c.*260dup ENSP00000462002.1:n.*260dup
ENST00000582761.1:c.108dup ENSP00000462909.1:p.Glu37Ter
ENST00000584865.5:n.286dup
NM_000789.3:c.2340dup NP_000780.1:p.Glu781Ter
NM_001178057.1:c.618dup NP_001171528.1:p.Glu207Ter
NM_152830.2:c.618dup NP_690043.1:p.Glu207Ter
XM_005257110.1:c.1791dup XP_005257167.1:p.Glu598Ter
XM_006721737.2:c.678dup XP_006721800.2:p.Glu227Ter
XM_006721737.3:c.678dup XP_006721800.2:p.Glu227Ter
NM_000789.4:c.2340dup MANE Select NP_000780.1:p.Glu781Ter
NM_001178057.2:c.618dup NP_001171528.1:p.Glu207Ter
NM_152830.3:c.618dup NP_690043.1:p.Glu207Ter
NM_001382700.1:c.1773dup NP_001369629.1:p.Glu592Ter
NM_001382701.1:c.1488dup NP_001369630.1:p.Glu497Ter
NM_001382702.1:c.270dup NP_001369631.1:p.Glu91Ter
NR_168483.1:n.718dup