Canonical Allele Identifier: CA2269950035

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497281G= , CM000679.2:g.63497281G=	GRCh38
NC_000017.10:g.61574642G= , CM000679.1:g.61574642G=	GRCh37
NC_000017.9:g.58928374G=	NCBI36
NG_011648.1:g.25209G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3836G= MANE Select	ENSP00000290866.4:p.Arg1279=
ENST00000290863.10:c.2114G=	ENSP00000290863.6:p.Arg705=
ENST00000290866.9:c.3836G=	ENSP00000290866.4:p.Arg1279=
ENST00000413513.7:c.1991G=	ENSP00000392247.3:p.Arg664=
ENST00000428043.5:c.*258G=	ENSP00000397593.2:n.*258G=
ENST00000577647.2:c.1969+296G=	ENSP00000464149.1:n.1969+296G=
ENST00000578839.5:c.*1591G=	ENSP00000462110.2:n.*1591G=
ENST00000579314.5:c.*1565G=	ENSP00000462599.1:n.*1565G=
NM_000789.3:c.3836G=	NP_000780.1:p.Arg1279=
NM_001178057.1:c.1991G=	NP_001171528.1:p.Arg664=
NM_152830.2:c.2114G=	NP_690043.1:p.Arg705=
XM_005257110.1:c.3287G=	XP_005257167.1:p.Arg1096=
XM_006721737.2:c.2174G=	XP_006721800.2:p.Arg725=
XM_006721737.3:c.2174G=	XP_006721800.2:p.Arg725=
NM_000789.4:c.3836G= MANE Select	NP_000780.1:p.Arg1279=
NM_001178057.2:c.1991G=	NP_001171528.1:p.Arg664=
NM_152830.3:c.2114G=	NP_690043.1:p.Arg705=
NM_001382700.1:c.3269G=	NP_001369629.1:p.Arg1090=
NM_001382701.1:c.2984G=	NP_001369630.1:p.Arg995=
NM_001382702.1:c.1451G=	NP_001369631.1:p.Arg484=
NR_168483.1:n.2214G=