Canonical Allele Identifier: CA2269946104

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488995A= , CM000679.2:g.63488995A=	GRCh38
NC_000017.10:g.61566356A= , CM000679.1:g.61566356A=	GRCh37
NC_000017.9:g.58920088A=	NCBI36
NG_011648.1:g.16923A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2504A= MANE Select	ENSP00000290866.4:p.Glu835=
ENST00000290863.10:c.782A=	ENSP00000290863.6:p.Glu261=
ENST00000290866.9:c.2504A=	ENSP00000290866.4:p.Glu835=
ENST00000413513.7:c.782A=	ENSP00000392247.3:p.Glu261=
ENST00000428043.5:c.2504A=	ENSP00000397593.2:p.Glu835=
ENST00000577647.2:c.782A=	ENSP00000464149.1:p.Glu261=
ENST00000578839.5:c.*519+204A=	ENSP00000462110.2:n.*519+204A=
ENST00000579204.1:c.763A=	ENSP00000464629.1:n.763A=
ENST00000579314.5:c.*233A=	ENSP00000462599.1:n.*233A=
ENST00000582005.5:c.*424A=	ENSP00000462002.1:n.*424A=
ENST00000582761.1:c.272A=	ENSP00000462909.1:p.Glu91=
ENST00000584865.5:n.450A=
NM_000789.3:c.2504A=	NP_000780.1:p.Glu835=
NM_001178057.1:c.782A=	NP_001171528.1:p.Glu261=
NM_152830.2:c.782A=	NP_690043.1:p.Glu261=
XM_005257110.1:c.1955A=	XP_005257167.1:p.Glu652=
XM_006721737.2:c.842A=	XP_006721800.2:p.Glu281=
XM_006721737.3:c.842A=	XP_006721800.2:p.Glu281=
NM_000789.4:c.2504A= MANE Select	NP_000780.1:p.Glu835=
NM_001178057.2:c.782A=	NP_001171528.1:p.Glu261=
NM_152830.3:c.782A=	NP_690043.1:p.Glu261=
NM_001382700.1:c.1937A=	NP_001369629.1:p.Glu646=
NM_001382701.1:c.1652A=	NP_001369630.1:p.Glu551=
NM_001382702.1:c.379+204A=	NP_001369631.1:n.379+204A=
NR_168483.1:n.882A=