Canonical Allele Identifier: CA2580575512
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63483402T>G , CM000679.2:g.63483402T>G GRCh38
NC_000017.10:g.61560763T>G , CM000679.1:g.61560763T>G GRCh37
NC_000017.9:g.58914495T>G NCBI36
NG_011648.1:g.11330T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.1488-58T>G MANE Select ENSP00000290866.4:n.1488-58T>G
ENST00000290866.9:c.1488-58T>G ENSP00000290866.4:n.1488-58T>G
ENST00000428043.5:c.1488-58T>G ENSP00000397593.2:n.1488-58T>G
ENST00000582678.5:c.*887-58T>G ENSP00000462995.1:n.*887-58T>G
ENST00000584529.5:n.1377-58T>G
NM_000789.3:c.1488-58T>G NP_000780.1:n.1488-58T>G
XM_005257110.1:c.939-58T>G XP_005257167.1:n.939-58T>G
NM_000789.4:c.1488-58T>G MANE Select NP_000780.1:n.1488-58T>G
NM_001382700.1:c.921-58T>G NP_001369629.1:n.921-58T>G
NM_001382701.1:c.636-58T>G NP_001369630.1:n.636-58T>G