Canonical Allele Identifier: CA2639261576
Gene: ACE HGNC NCBI

Linked Data

gnomAD v4: 17-63483695-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63483695G>A , CM000679.2:g.63483695G>A GRCh38
NC_000017.10:g.61561056G>A , CM000679.1:g.61561056G>A GRCh37
NC_000017.9:g.58914788G>A NCBI36
NG_011648.1:g.11623G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.1586+137G>A MANE Select ENSP00000290866.4:n.1586+137G>A
ENST00000290866.9:c.1586+137G>A ENSP00000290866.4:n.1586+137G>A
ENST00000428043.5:c.1586+137G>A ENSP00000397593.2:n.1586+137G>A
ENST00000582678.5:c.*985+137G>A ENSP00000462995.1:n.*985+137G>A
NM_000789.3:c.1586+137G>A NP_000780.1:n.1586+137G>A
XM_005257110.1:c.1037+137G>A XP_005257167.1:n.1037+137G>A
NM_000789.4:c.1586+137G>A MANE Select NP_000780.1:n.1586+137G>A
NM_001382700.1:c.1019+137G>A NP_001369629.1:n.1019+137G>A
NM_001382701.1:c.734+137G>A NP_001369630.1:n.734+137G>A
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