Canonical Allele Identifier: CA400557831
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63488671T>C , CM000679.2:g.63488671T>C GRCh38
NC_000017.10:g.61566032T>C , CM000679.1:g.61566032T>C GRCh37
NC_000017.9:g.58919764T>C NCBI36
NG_011648.1:g.16599T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.2329T>C MANE Select ENSP00000290866.4:p.Ser777Pro
ENST00000290863.10:c.607T>C ENSP00000290863.6:p.Ser203Pro
ENST00000290866.9:c.2329T>C ENSP00000290866.4:p.Ser777Pro
ENST00000413513.7:c.607T>C ENSP00000392247.3:p.Ser203Pro
ENST00000428043.5:c.2329T>C ENSP00000397593.2:p.Ser777Pro
ENST00000577647.2:c.607T>C ENSP00000464149.1:p.Ser203Pro
ENST00000578839.5:c.*399T>C ENSP00000462110.2:n.*399T>C
ENST00000579204.1:c.588T>C ENSP00000464629.1:n.588T>C
ENST00000579314.5:c.*58T>C ENSP00000462599.1:n.*58T>C
ENST00000582005.5:c.*249T>C ENSP00000462002.1:n.*249T>C
ENST00000582761.1:c.97T>C ENSP00000462909.1:p.Ser33Pro
ENST00000584865.5:n.275T>C
NM_000789.3:c.2329T>C NP_000780.1:p.Ser777Pro
NM_001178057.1:c.607T>C NP_001171528.1:p.Ser203Pro
NM_152830.2:c.607T>C NP_690043.1:p.Ser203Pro
XM_005257110.1:c.1780T>C XP_005257167.1:p.Ser594Pro
XM_006721737.2:c.667T>C XP_006721800.2:p.Ser223Pro
XM_006721737.3:c.667T>C XP_006721800.2:p.Ser223Pro
NM_000789.4:c.2329T>C MANE Select NP_000780.1:p.Ser777Pro
NM_001178057.2:c.607T>C NP_001171528.1:p.Ser203Pro
NM_152830.3:c.607T>C NP_690043.1:p.Ser203Pro
NM_001382700.1:c.1762T>C NP_001369629.1:p.Ser588Pro
NM_001382701.1:c.1477T>C NP_001369630.1:p.Ser493Pro
NM_001382702.1:c.259T>C NP_001369631.1:p.Ser87Pro
NR_168483.1:n.707T>C