Canonical Allele Identifier: CA400557849
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63488680T>C , CM000679.2:g.63488680T>C GRCh38
NC_000017.10:g.61566041T>C , CM000679.1:g.61566041T>C GRCh37
NC_000017.9:g.58919773T>C NCBI36
NG_011648.1:g.16608T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.2338T>C MANE Select ENSP00000290866.4:p.Tyr780His
ENST00000290863.10:c.616T>C ENSP00000290863.6:p.Tyr206His
ENST00000290866.9:c.2338T>C ENSP00000290866.4:p.Tyr780His
ENST00000413513.7:c.616T>C ENSP00000392247.3:p.Tyr206His
ENST00000428043.5:c.2338T>C ENSP00000397593.2:p.Tyr780His
ENST00000577647.2:c.616T>C ENSP00000464149.1:p.Tyr206His
ENST00000578839.5:c.*408T>C ENSP00000462110.2:n.*408T>C
ENST00000579204.1:c.597T>C ENSP00000464629.1:n.597T>C
ENST00000579314.5:c.*67T>C ENSP00000462599.1:n.*67T>C
ENST00000582005.5:c.*258T>C ENSP00000462002.1:n.*258T>C
ENST00000582761.1:c.106T>C ENSP00000462909.1:p.Tyr36His
ENST00000584865.5:n.284T>C
NM_000789.3:c.2338T>C NP_000780.1:p.Tyr780His
NM_001178057.1:c.616T>C NP_001171528.1:p.Tyr206His
NM_152830.2:c.616T>C NP_690043.1:p.Tyr206His
XM_005257110.1:c.1789T>C XP_005257167.1:p.Tyr597His
XM_006721737.2:c.676T>C XP_006721800.2:p.Tyr226His
XM_006721737.3:c.676T>C XP_006721800.2:p.Tyr226His
NM_000789.4:c.2338T>C MANE Select NP_000780.1:p.Tyr780His
NM_001178057.2:c.616T>C NP_001171528.1:p.Tyr206His
NM_152830.3:c.616T>C NP_690043.1:p.Tyr206His
NM_001382700.1:c.1771T>C NP_001369629.1:p.Tyr591His
NM_001382701.1:c.1486T>C NP_001369630.1:p.Tyr496His
NM_001382702.1:c.268T>C NP_001369631.1:p.Tyr90His
NR_168483.1:n.716T>C