Canonical Allele Identifier: CA2733691984
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs2049746544
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63483417T>C , CM000679.2:g.63483417T>C GRCh38
NC_000017.10:g.61560778T>C , CM000679.1:g.61560778T>C GRCh37
NC_000017.9:g.58914510T>C NCBI36
NG_011648.1:g.11345T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.1488-43T>C MANE Select ENSP00000290866.4:n.1488-43T>C
ENST00000290866.9:c.1488-43T>C ENSP00000290866.4:n.1488-43T>C
ENST00000428043.5:c.1488-43T>C ENSP00000397593.2:n.1488-43T>C
ENST00000582678.5:c.*887-43T>C ENSP00000462995.1:n.*887-43T>C
ENST00000584529.5:n.1377-43T>C
NM_000789.3:c.1488-43T>C NP_000780.1:n.1488-43T>C
XM_005257110.1:c.939-43T>C XP_005257167.1:n.939-43T>C
NM_000789.4:c.1488-43T>C MANE Select NP_000780.1:n.1488-43T>C
NM_001382700.1:c.921-43T>C NP_001369629.1:n.921-43T>C
NM_001382701.1:c.636-43T>C NP_001369630.1:n.636-43T>C
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