Canonical Allele Identifier: CA2269939897
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63477265C= , CM000679.2:g.63477265C= GRCh38
NC_000017.10:g.61554626C= , CM000679.1:g.61554626C= GRCh37
NC_000017.9:g.58908358C= NCBI36
NG_011648.1:g.5193C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.171C= MANE Select ENSP00000290866.4:p.Ala57=
ENST00000290866.9:c.171C= ENSP00000290866.4:p.Ala57=
ENST00000428043.5:c.171C= ENSP00000397593.2:p.Ala57=
ENST00000579462.1:n.196C=
ENST00000582678.5:c.171C= ENSP00000462995.1:p.Ala57=
ENST00000583336.5:n.205C=
ENST00000584529.5:n.205C=
NM_000789.3:c.171C= NP_000780.1:p.Ala57=
XM_005257110.1:c.-285C= XP_005257167.1:n.-285C=
NM_000789.4:c.171C= MANE Select NP_000780.1:p.Ala57=
NM_001382700.1:c.-65C= NP_001369629.1:n.-65C=
NM_001382701.1:c.-444C= NP_001369630.1:n.-444C=