Canonical Allele Identifier: CA2269950007

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497217G= , CM000679.2:g.63497217G=	GRCh38
NC_000017.10:g.61574578G= , CM000679.1:g.61574578G=	GRCh37
NC_000017.9:g.58928310G=	NCBI36
NG_011648.1:g.25145G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3772G= MANE Select	ENSP00000290866.4:p.Gly1258=
ENST00000290863.10:c.2050G=	ENSP00000290863.6:p.Gly684=
ENST00000290866.9:c.3772G=	ENSP00000290866.4:p.Gly1258=
ENST00000413513.7:c.1927G=	ENSP00000392247.3:p.Gly643=
ENST00000428043.5:c.*194G=	ENSP00000397593.2:n.*194G=
ENST00000577647.2:c.1969+232G=	ENSP00000464149.1:n.1969+232G=
ENST00000578839.5:c.*1527G=	ENSP00000462110.2:n.*1527G=
ENST00000579314.5:c.*1501G=	ENSP00000462599.1:n.*1501G=
NM_000789.3:c.3772G=	NP_000780.1:p.Gly1258=
NM_001178057.1:c.1927G=	NP_001171528.1:p.Gly643=
NM_152830.2:c.2050G=	NP_690043.1:p.Gly684=
XM_005257110.1:c.3223G=	XP_005257167.1:p.Gly1075=
XM_006721737.2:c.2110G=	XP_006721800.2:p.Gly704=
XM_006721737.3:c.2110G=	XP_006721800.2:p.Gly704=
NM_000789.4:c.3772G= MANE Select	NP_000780.1:p.Gly1258=
NM_001178057.2:c.1927G=	NP_001171528.1:p.Gly643=
NM_152830.3:c.2050G=	NP_690043.1:p.Gly684=
NM_001382700.1:c.3205G=	NP_001369629.1:p.Gly1069=
NM_001382701.1:c.2920G=	NP_001369630.1:p.Gly974=
NM_001382702.1:c.1387G=	NP_001369631.1:p.Gly463=
NR_168483.1:n.2150G=