Canonical Allele Identifier: CA2269944879

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486683C= , CM000679.2:g.63486683C=	GRCh38
NC_000017.10:g.61564044C= , CM000679.1:g.61564044C=	GRCh37
NC_000017.9:g.58917776C=	NCBI36
NG_011648.1:g.14611C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2185C= MANE Select	ENSP00000290866.4:p.Arg729=
ENST00000290863.10:c.463C=	ENSP00000290863.6:p.Arg155=
ENST00000290866.9:c.2185C=	ENSP00000290866.4:p.Arg729=
ENST00000413513.7:c.463C=	ENSP00000392247.3:p.Arg155=
ENST00000428043.5:c.2185C=	ENSP00000397593.2:p.Arg729=
ENST00000577647.2:c.463C=	ENSP00000464149.1:p.Arg155=
ENST00000578839.5:c.*255C=	ENSP00000462110.2:n.*255C=
ENST00000579204.1:c.366C=	ENSP00000464629.1:n.366C=
ENST00000579314.5:c.463C=	ENSP00000462599.1:p.Arg155=
ENST00000579726.5:c.747C=
ENST00000582005.5:c.*105C=	ENSP00000462002.1:n.*105C=
NM_000789.3:c.2185C=	NP_000780.1:p.Arg729=
NM_001178057.1:c.463C=	NP_001171528.1:p.Arg155=
NM_152830.2:c.463C=	NP_690043.1:p.Arg155=
XM_005257110.1:c.1636C=	XP_005257167.1:p.Arg546=
XM_006721737.2:c.523C=	XP_006721800.2:p.Arg175=
XM_006721737.3:c.523C=	XP_006721800.2:p.Arg175=
NM_000789.4:c.2185C= MANE Select	NP_000780.1:p.Arg729=
NM_001178057.2:c.463C=	NP_001171528.1:p.Arg155=
NM_152830.3:c.463C=	NP_690043.1:p.Arg155=
NM_001382700.1:c.1618C=	NP_001369629.1:p.Arg540=
NM_001382701.1:c.1333C=	NP_001369630.1:p.Arg445=
NM_001382702.1:c.115C=	NP_001369631.1:p.Arg39=
NR_168483.1:n.485C=