Canonical Allele Identifier: CA2269942640

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63482567C= , CM000679.2:g.63482567C=	GRCh38
NC_000017.10:g.61559928C= , CM000679.1:g.61559928C=	GRCh37
NC_000017.9:g.58913660C=	NCBI36
NG_011648.1:g.10495C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.1220C= MANE Select	ENSP00000290866.4:p.Ser407=
ENST00000290866.9:c.1220C=	ENSP00000290866.4:p.Ser407=
ENST00000428043.5:c.1220C=	ENSP00000397593.2:p.Ser407=
ENST00000582678.5:c.*619C=	ENSP00000462995.1:n.*619C=
ENST00000584529.5:n.1254C=
NM_000789.3:c.1220C=	NP_000780.1:p.Ser407=
XM_005257110.1:c.671C=	XP_005257167.1:p.Ser224=
NM_000789.4:c.1220C= MANE Select	NP_000780.1:p.Ser407=
NM_001382700.1:c.653C=	NP_001369629.1:p.Ser218=
NM_001382701.1:c.368C=	NP_001369630.1:p.Ser123=