Canonical Allele Identifier: CA2269950626
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63498237_63498242delinsACACCT , CM000679.2:g.63498237_63498242delinsACACCT GRCh38
NC_000017.10:g.61575598_61575603delinsACACCT , CM000679.1:g.61575598_61575603delinsACACCT GRCh37
NC_000017.9:g.58929330_58929335delinsACACCT NCBI36
NG_011648.1:g.26165_26170delinsACACCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.*871_*876delinsACACCT MANE Select ENSP00000290866.4:n.*871_*876delinsACACCT
ENST00000290866.9:c.*871_*876delinsACACCT ENSP00000290866.4:n.*871_*876delinsACACCT
ENST00000428043.5:c.*1214_*1219delinsACACCT ENSP00000397593.2:n.*1214_*1219delinsACACCT
ENST00000577647.2:c.1969+1252_1969+1257delinsACACCT ENSP00000464149.1:n.1969+1252_1969+1257delinsACACCT
NM_000789.3:c.*871_*876delinsACACCT NP_000780.1:n.*871_*876delinsACACCT
NM_001178057.1:c.*871_*876delinsACACCT NP_001171528.1:n.*871_*876delinsACACCT
NM_152830.2:c.*871_*876delinsACACCT NP_690043.1:n.*871_*876delinsACACCT
XM_005257110.1:c.*871_*876delinsACACCT XP_005257167.1:n.*871_*876delinsACACCT
XM_006721737.2:c.*871_*876delinsACACCT XP_006721800.2:n.*871_*876delinsACACCT
NM_000789.4:c.*871_*876delinsACACCT MANE Select NP_000780.1:n.*871_*876delinsACACCT
NM_001178057.2:c.*871_*876delinsACACCT NP_001171528.1:n.*871_*876delinsACACCT
NM_152830.3:c.*871_*876delinsACACCT NP_690043.1:n.*871_*876delinsACACCT
NM_001382700.1:c.*871_*876delinsACACCT NP_001369629.1:n.*871_*876delinsACACCT
NM_001382701.1:c.*871_*876delinsACACCT NP_001369630.1:n.*871_*876delinsACACCT
NM_001382702.1:c.*871_*876delinsACACCT NP_001369631.1:n.*871_*876delinsACACCT
NR_168483.1:n.3170_3175delinsACACCT