Canonical Allele Identifier: CA2269942594
Gene: ACE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63482462C= , CM000679.2:g.63482462C= GRCh38
NC_000017.10:g.61559823C= , CM000679.1:g.61559823C= GRCh37
NC_000017.9:g.58913555C= NCBI36
NG_011648.1:g.10390C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.1119-4C= MANE Select ENSP00000290866.4:n.1119-4C=
ENST00000290866.9:c.1119-4C= ENSP00000290866.4:n.1119-4C=
ENST00000428043.5:c.1119-4C= ENSP00000397593.2:n.1119-4C=
ENST00000582678.5:c.*518-4C= ENSP00000462995.1:n.*518-4C=
ENST00000584529.5:n.1153-4C=
NM_000789.3:c.1119-4C= NP_000780.1:n.1119-4C=
XM_005257110.1:c.570-4C= XP_005257167.1:n.570-4C=
NM_000789.4:c.1119-4C= MANE Select NP_000780.1:n.1119-4C=
NM_001382700.1:c.548C= NP_001369629.1:p.Pro183=
NM_001382701.1:c.267-4C= NP_001369630.1:n.267-4C=
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