Canonical Allele Identifier: CA2269950562
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63498121_63498125delinsTCAGA , CM000679.2:g.63498121_63498125delinsTCAGA GRCh38
NC_000017.10:g.61575482_61575486delinsTCAGA , CM000679.1:g.61575482_61575486delinsTCAGA GRCh37
NC_000017.9:g.58929214_58929218delinsTCAGA NCBI36
NG_011648.1:g.26049_26053delinsTCAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.*755_*759delinsTCAGA MANE Select ENSP00000290866.4:n.*755_*759delinsTCAGA
ENST00000290866.9:c.*755_*759delinsTCAGA ENSP00000290866.4:n.*755_*759delinsTCAGA
ENST00000428043.5:c.*1098_*1102delinsTCAGA ENSP00000397593.2:n.*1098_*1102delinsTCAGA
ENST00000577647.2:c.1969+1136_1969+1140delinsTCAGA ENSP00000464149.1:n.1969+1136_1969+1140delinsTCAGA
NM_000789.3:c.*755_*759delinsTCAGA NP_000780.1:n.*755_*759delinsTCAGA
NM_001178057.1:c.*755_*759delinsTCAGA NP_001171528.1:n.*755_*759delinsTCAGA
NM_152830.2:c.*755_*759delinsTCAGA NP_690043.1:n.*755_*759delinsTCAGA
XM_005257110.1:c.*755_*759delinsTCAGA XP_005257167.1:n.*755_*759delinsTCAGA
XM_006721737.2:c.*755_*759delinsTCAGA XP_006721800.2:n.*755_*759delinsTCAGA
NM_000789.4:c.*755_*759delinsTCAGA MANE Select NP_000780.1:n.*755_*759delinsTCAGA
NM_001178057.2:c.*755_*759delinsTCAGA NP_001171528.1:n.*755_*759delinsTCAGA
NM_152830.3:c.*755_*759delinsTCAGA NP_690043.1:n.*755_*759delinsTCAGA
NM_001382700.1:c.*755_*759delinsTCAGA NP_001369629.1:n.*755_*759delinsTCAGA
NM_001382701.1:c.*755_*759delinsTCAGA NP_001369630.1:n.*755_*759delinsTCAGA
NM_001382702.1:c.*755_*759delinsTCAGA NP_001369631.1:n.*755_*759delinsTCAGA
NR_168483.1:n.3054_3058delinsTCAGA