Canonical Allele Identifier: CA292877480
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs35650564
MyVariant Identifiers: chr17:g.61560789del (hg19) chr17:g.63483428del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63483429del , CM000679.2:g.63483429del GRCh38
NC_000017.10:g.61560790del , CM000679.1:g.61560790del GRCh37
NC_000017.9:g.58914522del NCBI36
NG_011648.1:g.11357del

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.1488-31del MANE Select ENSP00000290866.4:n.1488-31del
ENST00000290866.9:c.1488-31del ENSP00000290866.4:n.1488-31del
ENST00000428043.5:c.1488-31del ENSP00000397593.2:n.1488-31del
ENST00000582678.5:c.*887-31del ENSP00000462995.1:n.*887-31del
ENST00000584529.5:n.1377-31del
NM_000789.3:c.1488-31del NP_000780.1:n.1488-31del
XM_005257110.1:c.939-31del XP_005257167.1:n.939-31del
NM_000789.4:c.1488-31del MANE Select NP_000780.1:n.1488-31del
NM_001382700.1:c.921-31del NP_001369629.1:n.921-31del
NM_001382701.1:c.636-31del NP_001369630.1:n.636-31del
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