Canonical Allele Identifier: CA2269949994

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497191A= , CM000679.2:g.63497191A=	GRCh38
NC_000017.10:g.61574552A= , CM000679.1:g.61574552A=	GRCh37
NC_000017.9:g.58928284A=	NCBI36
NG_011648.1:g.25119A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3746A= MANE Select	ENSP00000290866.4:p.Asp1249=
ENST00000290863.10:c.2024A=	ENSP00000290863.6:p.Asp675=
ENST00000290866.9:c.3746A=	ENSP00000290866.4:p.Asp1249=
ENST00000413513.7:c.1901A=	ENSP00000392247.3:p.Asp634=
ENST00000428043.5:c.*168A=	ENSP00000397593.2:n.*168A=
ENST00000577647.2:c.1969+206A=	ENSP00000464149.1:n.1969+206A=
ENST00000578839.5:c.*1501A=	ENSP00000462110.2:n.*1501A=
ENST00000579314.5:c.*1475A=	ENSP00000462599.1:n.*1475A=
NM_000789.3:c.3746A=	NP_000780.1:p.Asp1249=
NM_001178057.1:c.1901A=	NP_001171528.1:p.Asp634=
NM_152830.2:c.2024A=	NP_690043.1:p.Asp675=
XM_005257110.1:c.3197A=	XP_005257167.1:p.Asp1066=
XM_006721737.2:c.2084A=	XP_006721800.2:p.Asp695=
XM_006721737.3:c.2084A=	XP_006721800.2:p.Asp695=
NM_000789.4:c.3746A= MANE Select	NP_000780.1:p.Asp1249=
NM_001178057.2:c.1901A=	NP_001171528.1:p.Asp634=
NM_152830.3:c.2024A=	NP_690043.1:p.Asp675=
NM_001382700.1:c.3179A=	NP_001369629.1:p.Asp1060=
NM_001382701.1:c.2894A=	NP_001369630.1:p.Asp965=
NM_001382702.1:c.1361A=	NP_001369631.1:p.Asp454=
NR_168483.1:n.2124A=