Canonical Allele Identifier: CA8699135

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63479806C>G , CM000679.2:g.63479806C>G	GRCh38
NC_000017.10:g.61557167C>G , CM000679.1:g.61557167C>G	GRCh37
NC_000017.9:g.58910899C>G	NCBI36
NG_011648.1:g.7734C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.549C>G MANE Select	ENSP00000290866.4:p.Ala183=
ENST00000290866.9:c.549C>G	ENSP00000290866.4:p.Ala183=
ENST00000428043.5:c.549C>G	ENSP00000397593.2:p.Ala183=
ENST00000580318.1:n.738C>G
ENST00000582627.1:c.549C>G	ENSP00000462280.1:p.Ala183=
ENST00000582678.5:c.455C>G	ENSP00000462995.1:p.Pro152Arg
ENST00000584529.5:n.583C>G
NM_000789.3:c.549C>G	NP_000780.1:p.Ala183=
XM_005257110.1:c.-1C>G	XP_005257167.1:n.-1C>G
NM_000789.4:c.549C>G MANE Select	NP_000780.1:p.Ala183=
NM_001382700.1:c.183-531C>G	NP_001369629.1:n.183-531C>G
NM_001382701.1:c.-197-531C>G	NP_001369630.1:n.-197-531C>G