Canonical Allele Identifier: CA2639261639
Gene: ACE HGNC NCBI

Linked Data

gnomAD v4: 17-63483810-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63483810C>A , CM000679.2:g.63483810C>A GRCh38
NC_000017.10:g.61561171C>A , CM000679.1:g.61561171C>A GRCh37
NC_000017.9:g.58914903C>A NCBI36
NG_011648.1:g.11738C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.1587-39C>A MANE Select ENSP00000290866.4:n.1587-39C>A
ENST00000290866.9:c.1587-39C>A ENSP00000290866.4:n.1587-39C>A
ENST00000428043.5:c.1587-39C>A ENSP00000397593.2:n.1587-39C>A
ENST00000582678.5:c.*986-39C>A ENSP00000462995.1:n.*986-39C>A
NM_000789.3:c.1587-39C>A NP_000780.1:n.1587-39C>A
XM_005257110.1:c.1038-39C>A XP_005257167.1:n.1038-39C>A
NM_000789.4:c.1587-39C>A MANE Select NP_000780.1:n.1587-39C>A
NM_001382700.1:c.1020-39C>A NP_001369629.1:n.1020-39C>A
NM_001382701.1:c.735-39C>A NP_001369630.1:n.735-39C>A
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