Canonical Allele Identifier: CA400540344
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs1168795526

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63477758C>G , CM000679.2:g.63477758C>G GRCh38
NC_000017.10:g.61555119C>G , CM000679.1:g.61555119C>G GRCh37
NC_000017.9:g.58908851C>G NCBI36
NG_011648.1:g.5686C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.250-173C>G MANE Select ENSP00000290866.4:n.250-173C>G
ENST00000290866.9:c.250-173C>G ENSP00000290866.4:n.250-173C>G
ENST00000428043.5:c.250-173C>G ENSP00000397593.2:n.250-173C>G
ENST00000579462.1:n.275-173C>G
ENST00000580318.1:n.266C>G
ENST00000582627.1:c.217C>G ENSP00000462280.1:p.Gln73Glu
ENST00000582678.5:c.250-173C>G ENSP00000462995.1:n.250-173C>G
ENST00000583336.5:n.284-173C>G
ENST00000584529.5:n.284-173C>G
NM_000789.3:c.250-173C>G NP_000780.1:n.250-173C>G
XM_005257110.1:c.-206-173C>G XP_005257167.1:n.-206-173C>G
NM_000789.4:c.250-173C>G MANE Select NP_000780.1:n.250-173C>G
NM_001382700.1:c.15-173C>G NP_001369629.1:n.15-173C>G
NM_001382701.1:c.-365-173C>G NP_001369630.1:n.-365-173C>G