Canonical Allele Identifier: CA2269950041

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497296G= , CM000679.2:g.63497296G=	GRCh38
NC_000017.10:g.61574657G= , CM000679.1:g.61574657G=	GRCh37
NC_000017.9:g.58928389G=	NCBI36
NG_011648.1:g.25224G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3851G= MANE Select	ENSP00000290866.4:p.Arg1284=
ENST00000290863.10:c.2129G=	ENSP00000290863.6:p.Arg710=
ENST00000290866.9:c.3851G=	ENSP00000290866.4:p.Arg1284=
ENST00000413513.7:c.2006G=	ENSP00000392247.3:p.Arg669=
ENST00000428043.5:c.*273G=	ENSP00000397593.2:n.*273G=
ENST00000577647.2:c.1969+311G=	ENSP00000464149.1:n.1969+311G=
ENST00000578839.5:c.*1606G=	ENSP00000462110.2:n.*1606G=
ENST00000579314.5:c.*1580G=	ENSP00000462599.1:n.*1580G=
NM_000789.3:c.3851G=	NP_000780.1:p.Arg1284=
NM_001178057.1:c.2006G=	NP_001171528.1:p.Arg669=
NM_152830.2:c.2129G=	NP_690043.1:p.Arg710=
XM_005257110.1:c.3302G=	XP_005257167.1:p.Arg1101=
XM_006721737.2:c.2189G=	XP_006721800.2:p.Arg730=
XM_006721737.3:c.2189G=	XP_006721800.2:p.Arg730=
NM_000789.4:c.3851G= MANE Select	NP_000780.1:p.Arg1284=
NM_001178057.2:c.2006G=	NP_001171528.1:p.Arg669=
NM_152830.3:c.2129G=	NP_690043.1:p.Arg710=
NM_001382700.1:c.3284G=	NP_001369629.1:p.Arg1095=
NM_001382701.1:c.2999G=	NP_001369630.1:p.Arg1000=
NM_001382702.1:c.1466G=	NP_001369631.1:p.Arg489=
NR_168483.1:n.2229G=