Canonical Allele Identifier: CA2269941679
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63480815C= , CM000679.2:g.63480815C= GRCh38
NC_000017.10:g.61558176C= , CM000679.1:g.61558176C= GRCh37
NC_000017.9:g.58911908C= NCBI36
NG_011648.1:g.8743C=

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.848-276C= MANE Select ENSP00000290866.4:n.848-276C=
ENST00000290866.9:c.848-276C= ENSP00000290866.4:n.848-276C=
ENST00000428043.5:c.848-276C= ENSP00000397593.2:n.848-276C=
ENST00000582627.1:c.848-276C= ENSP00000462280.1:n.848-276C=
ENST00000582678.5:c.*247-276C= ENSP00000462995.1:n.*247-276C=
ENST00000584529.5:n.882-276C=
NM_000789.3:c.848-276C= NP_000780.1:n.848-276C=
XM_005257110.1:c.299-276C= XP_005257167.1:n.299-276C=
NM_000789.4:c.848-276C= MANE Select NP_000780.1:n.848-276C=
NM_001382700.1:c.375-276C= NP_001369629.1:n.375-276C=
NM_001382701.1:c.-5-276C= NP_001369630.1:n.-5-276C=