Canonical Allele Identifier: CA8699035
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs556087296

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63478091G>A , CM000679.2:g.63478091G>A GRCh38
NC_000017.10:g.61555452G>A , CM000679.1:g.61555452G>A GRCh37
NC_000017.9:g.58909184G>A NCBI36
NG_011648.1:g.6019G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.410G>A MANE Select ENSP00000290866.4:p.Arg137Gln
ENST00000290866.9:c.410G>A ENSP00000290866.4:p.Arg137Gln
ENST00000428043.5:c.410G>A ENSP00000397593.2:p.Arg137Gln
ENST00000579462.1:n.435G>A
ENST00000580318.1:n.599G>A
ENST00000582627.1:c.410G>A ENSP00000462280.1:p.Arg137Gln
ENST00000582678.5:c.410G>A ENSP00000462995.1:p.Arg137Gln
ENST00000583336.5:n.444G>A
ENST00000584529.5:n.444G>A
NM_000789.3:c.410G>A NP_000780.1:p.Arg137Gln
XM_005257110.1:c.-46G>A XP_005257167.1:n.-46G>A
NM_000789.4:c.410G>A MANE Select NP_000780.1:p.Arg137Gln
NM_001382700.1:c.175G>A NP_001369629.1:p.Gly59Ser
NM_001382701.1:c.-205G>A NP_001369630.1:n.-205G>A