Canonical Allele Identifier: CA2269945939
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63488674C= , CM000679.2:g.63488674C= GRCh38
NC_000017.10:g.61566035C= , CM000679.1:g.61566035C= GRCh37
NC_000017.9:g.58919767C= NCBI36
NG_011648.1:g.16602C=

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.2332C= MANE Select ENSP00000290866.4:p.Arg778=
ENST00000290863.10:c.610C= ENSP00000290863.6:p.Arg204=
ENST00000290866.9:c.2332C= ENSP00000290866.4:p.Arg778=
ENST00000413513.7:c.610C= ENSP00000392247.3:p.Arg204=
ENST00000428043.5:c.2332C= ENSP00000397593.2:p.Arg778=
ENST00000577647.2:c.610C= ENSP00000464149.1:p.Arg204=
ENST00000578839.5:c.*402C= ENSP00000462110.2:n.*402C=
ENST00000579204.1:c.591C= ENSP00000464629.1:n.591C=
ENST00000579314.5:c.*61C= ENSP00000462599.1:n.*61C=
ENST00000582005.5:c.*252C= ENSP00000462002.1:n.*252C=
ENST00000582761.1:c.100C= ENSP00000462909.1:p.Arg34=
ENST00000584865.5:n.278C=
NM_000789.3:c.2332C= NP_000780.1:p.Arg778=
NM_001178057.1:c.610C= NP_001171528.1:p.Arg204=
NM_152830.2:c.610C= NP_690043.1:p.Arg204=
XM_005257110.1:c.1783C= XP_005257167.1:p.Arg595=
XM_006721737.2:c.670C= XP_006721800.2:p.Arg224=
XM_006721737.3:c.670C= XP_006721800.2:p.Arg224=
NM_000789.4:c.2332C= MANE Select NP_000780.1:p.Arg778=
NM_001178057.2:c.610C= NP_001171528.1:p.Arg204=
NM_152830.3:c.610C= NP_690043.1:p.Arg204=
NM_001382700.1:c.1765C= NP_001369629.1:p.Arg589=
NM_001382701.1:c.1480C= NP_001369630.1:p.Arg494=
NM_001382702.1:c.262C= NP_001369631.1:p.Arg88=
NR_168483.1:n.710C=