Canonical Allele Identifier: CA2269943323
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs2029861315
gnomAD v4: 17-63483795-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63483799del , CM000679.2:g.63483799del GRCh38
NC_000017.10:g.61561160del , CM000679.1:g.61561160del GRCh37
NC_000017.9:g.58914892del NCBI36
NG_011648.1:g.11727del

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.1587-50del MANE Select ENSP00000290866.4:n.1587-50del
ENST00000290866.9:c.1587-50del ENSP00000290866.4:n.1587-50del
ENST00000428043.5:c.1587-50del ENSP00000397593.2:n.1587-50del
ENST00000582678.5:c.*986-50del ENSP00000462995.1:n.*986-50del
NM_000789.3:c.1587-50del NP_000780.1:n.1587-50del
XM_005257110.1:c.1038-50del XP_005257167.1:n.1038-50del
NM_000789.4:c.1587-50del MANE Select NP_000780.1:n.1587-50del
NM_001382700.1:c.1020-50del NP_001369629.1:n.1020-50del
NM_001382701.1:c.735-50del NP_001369630.1:n.735-50del
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