Canonical Allele Identifier: CA2639261626
Gene: ACE HGNC NCBI

Linked Data

gnomAD v4: 17-63483776-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63483776G>C , CM000679.2:g.63483776G>C GRCh38
NC_000017.10:g.61561137G>C , CM000679.1:g.61561137G>C GRCh37
NC_000017.9:g.58914869G>C NCBI36
NG_011648.1:g.11704G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.1587-73G>C MANE Select ENSP00000290866.4:n.1587-73G>C
ENST00000290866.9:c.1587-73G>C ENSP00000290866.4:n.1587-73G>C
ENST00000428043.5:c.1587-73G>C ENSP00000397593.2:n.1587-73G>C
ENST00000582678.5:c.*986-73G>C ENSP00000462995.1:n.*986-73G>C
NM_000789.3:c.1587-73G>C NP_000780.1:n.1587-73G>C
XM_005257110.1:c.1038-73G>C XP_005257167.1:n.1038-73G>C
NM_000789.4:c.1587-73G>C MANE Select NP_000780.1:n.1587-73G>C
NM_001382700.1:c.1020-73G>C NP_001369629.1:n.1020-73G>C
NM_001382701.1:c.735-73G>C NP_001369630.1:n.735-73G>C
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