Canonical Allele Identifier: CA2269946118

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63489019A= , CM000679.2:g.63489019A=	GRCh38
NC_000017.10:g.61566380A= , CM000679.1:g.61566380A=	GRCh37
NC_000017.9:g.58920112A=	NCBI36
NG_011648.1:g.16947A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2528A= MANE Select	ENSP00000290866.4:p.Gln843=
ENST00000290863.10:c.806A=	ENSP00000290863.6:p.Gln269=
ENST00000290866.9:c.2528A=	ENSP00000290866.4:p.Gln843=
ENST00000413513.7:c.806A=	ENSP00000392247.3:p.Gln269=
ENST00000428043.5:c.2528A=	ENSP00000397593.2:p.Gln843=
ENST00000577647.2:c.806A=	ENSP00000464149.1:p.Gln269=
ENST00000578839.5:c.*519+228A=	ENSP00000462110.2:n.*519+228A=
ENST00000579204.1:c.787A=	ENSP00000464629.1:n.787A=
ENST00000579314.5:c.*257A=	ENSP00000462599.1:n.*257A=
ENST00000582005.5:c.*448A=	ENSP00000462002.1:n.*448A=
ENST00000582761.1:c.296A=	ENSP00000462909.1:p.Gln99=
ENST00000584865.5:n.474A=
NM_000789.3:c.2528A=	NP_000780.1:p.Gln843=
NM_001178057.1:c.806A=	NP_001171528.1:p.Gln269=
NM_152830.2:c.806A=	NP_690043.1:p.Gln269=
XM_005257110.1:c.1979A=	XP_005257167.1:p.Gln660=
XM_006721737.2:c.866A=	XP_006721800.2:p.Gln289=
XM_006721737.3:c.866A=	XP_006721800.2:p.Gln289=
NM_000789.4:c.2528A= MANE Select	NP_000780.1:p.Gln843=
NM_001178057.2:c.806A=	NP_001171528.1:p.Gln269=
NM_152830.3:c.806A=	NP_690043.1:p.Gln269=
NM_001382700.1:c.1961A=	NP_001369629.1:p.Gln654=
NM_001382701.1:c.1676A=	NP_001369630.1:p.Gln559=
NM_001382702.1:c.379+228A=	NP_001369631.1:n.379+228A=
NR_168483.1:n.906A=