Canonical Allele Identifier: CA2269949777

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496857G= , CM000679.2:g.63496857G=	GRCh38
NC_000017.10:g.61574218G= , CM000679.1:g.61574218G=	GRCh37
NC_000017.9:g.58927950G=	NCBI36
NG_011648.1:g.24785G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3563G= MANE Select	ENSP00000290866.4:p.Gly1188=
ENST00000290863.10:c.1841G=	ENSP00000290863.6:p.Gly614=
ENST00000290866.9:c.3563G=	ENSP00000290866.4:p.Gly1188=
ENST00000413513.7:c.1718G=	ENSP00000392247.3:p.Gly573=
ENST00000428043.5:c.3563G=	ENSP00000397593.2:p.Gly1188=
ENST00000577418.5:n.573G=
ENST00000577647.2:c.1841G=	ENSP00000464149.1:p.Gly614=
ENST00000578839.5:c.*1318G=	ENSP00000462110.2:n.*1318G=
ENST00000579314.5:c.*1292G=	ENSP00000462599.1:n.*1292G=
ENST00000579409.1:c.250G=
ENST00000582244.1:n.437G=
NM_000789.3:c.3563G=	NP_000780.1:p.Gly1188=
NM_001178057.1:c.1718G=	NP_001171528.1:p.Gly573=
NM_152830.2:c.1841G=	NP_690043.1:p.Gly614=
XM_005257110.1:c.3014G=	XP_005257167.1:p.Gly1005=
XM_006721737.2:c.1901G=	XP_006721800.2:p.Gly634=
XM_006721737.3:c.1901G=	XP_006721800.2:p.Gly634=
NM_000789.4:c.3563G= MANE Select	NP_000780.1:p.Gly1188=
NM_001178057.2:c.1718G=	NP_001171528.1:p.Gly573=
NM_152830.3:c.1841G=	NP_690043.1:p.Gly614=
NM_001382700.1:c.2996G=	NP_001369629.1:p.Gly999=
NM_001382701.1:c.2711G=	NP_001369630.1:p.Gly904=
NM_001382702.1:c.1178G=	NP_001369631.1:p.Gly393=
NR_168483.1:n.1941G=