Canonical Allele Identifier: CA2269950020

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497249C= , CM000679.2:g.63497249C=	GRCh38
NC_000017.10:g.61574610C= , CM000679.1:g.61574610C=	GRCh37
NC_000017.9:g.58928342C=	NCBI36
NG_011648.1:g.25177C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3804C= MANE Select	ENSP00000290866.4:p.Ala1268=
ENST00000290863.10:c.2082C=	ENSP00000290863.6:p.Ala694=
ENST00000290866.9:c.3804C=	ENSP00000290866.4:p.Ala1268=
ENST00000413513.7:c.1959C=	ENSP00000392247.3:p.Ala653=
ENST00000428043.5:c.*226C=	ENSP00000397593.2:n.*226C=
ENST00000577647.2:c.1969+264C=	ENSP00000464149.1:n.1969+264C=
ENST00000578839.5:c.*1559C=	ENSP00000462110.2:n.*1559C=
ENST00000579314.5:c.*1533C=	ENSP00000462599.1:n.*1533C=
NM_000789.3:c.3804C=	NP_000780.1:p.Ala1268=
NM_001178057.1:c.1959C=	NP_001171528.1:p.Ala653=
NM_152830.2:c.2082C=	NP_690043.1:p.Ala694=
XM_005257110.1:c.3255C=	XP_005257167.1:p.Ala1085=
XM_006721737.2:c.2142C=	XP_006721800.2:p.Ala714=
XM_006721737.3:c.2142C=	XP_006721800.2:p.Ala714=
NM_000789.4:c.3804C= MANE Select	NP_000780.1:p.Ala1268=
NM_001178057.2:c.1959C=	NP_001171528.1:p.Ala653=
NM_152830.3:c.2082C=	NP_690043.1:p.Ala694=
NM_001382700.1:c.3237C=	NP_001369629.1:p.Ala1079=
NM_001382701.1:c.2952C=	NP_001369630.1:p.Ala984=
NM_001382702.1:c.1419C=	NP_001369631.1:p.Ala473=
NR_168483.1:n.2182C=