Canonical Allele Identifier: CA2269944890

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486701C= , CM000679.2:g.63486701C=	GRCh38
NC_000017.10:g.61564062C= , CM000679.1:g.61564062C=	GRCh37
NC_000017.9:g.58917794C=	NCBI36
NG_011648.1:g.14629C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2203C= MANE Select	ENSP00000290866.4:p.Gln735=
ENST00000290863.10:c.481C=	ENSP00000290863.6:p.Gln161=
ENST00000290866.9:c.2203C=	ENSP00000290866.4:p.Gln735=
ENST00000413513.7:c.481C=	ENSP00000392247.3:p.Gln161=
ENST00000428043.5:c.2203C=	ENSP00000397593.2:p.Gln735=
ENST00000577647.2:c.481C=	ENSP00000464149.1:p.Gln161=
ENST00000578839.5:c.*273C=	ENSP00000462110.2:n.*273C=
ENST00000579204.1:c.384C=	ENSP00000464629.1:n.384C=
ENST00000579314.5:c.481C=	ENSP00000462599.1:p.Gln161=
ENST00000579726.5:c.765C=
ENST00000582005.5:c.*123C=	ENSP00000462002.1:n.*123C=
NM_000789.3:c.2203C=	NP_000780.1:p.Gln735=
NM_001178057.1:c.481C=	NP_001171528.1:p.Gln161=
NM_152830.2:c.481C=	NP_690043.1:p.Gln161=
XM_005257110.1:c.1654C=	XP_005257167.1:p.Gln552=
XM_006721737.2:c.541C=	XP_006721800.2:p.Gln181=
XM_006721737.3:c.541C=	XP_006721800.2:p.Gln181=
NM_000789.4:c.2203C= MANE Select	NP_000780.1:p.Gln735=
NM_001178057.2:c.481C=	NP_001171528.1:p.Gln161=
NM_152830.3:c.481C=	NP_690043.1:p.Gln161=
NM_001382700.1:c.1636C=	NP_001369629.1:p.Gln546=
NM_001382701.1:c.1351C=	NP_001369630.1:p.Gln451=
NM_001382702.1:c.133C=	NP_001369631.1:p.Gln45=
NR_168483.1:n.503C=