Canonical Allele Identifier: CA2810114705

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498364dup , CM000679.2:g.63498364dup	GRCh38
NC_000017.10:g.61575725dup , CM000679.1:g.61575725dup	GRCh37
NC_000017.9:g.58929457dup	NCBI36
NG_011648.1:g.26292dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*998dup MANE Select	ENSP00000290866.4:n.*998dup
ENST00000290866.9:c.*998dup	ENSP00000290866.4:n.*998dup
ENST00000428043.5:c.*1341dup	ENSP00000397593.2:n.*1341dup
ENST00000577647.2:c.1969+1379dup	ENSP00000464149.1:n.1969+1379dup
NM_000789.3:c.*998dup	NP_000780.1:n.*998dup
NM_001178057.1:c.*998dup	NP_001171528.1:n.*998dup
NM_152830.2:c.*998dup	NP_690043.1:n.*998dup
XM_005257110.1:c.*998dup	XP_005257167.1:n.*998dup
XM_006721737.2:c.*998dup	XP_006721800.2:n.*998dup
NM_000789.4:c.*998dup MANE Select	NP_000780.1:n.*998dup
NM_001178057.2:c.*998dup	NP_001171528.1:n.*998dup
NM_152830.3:c.*998dup	NP_690043.1:n.*998dup
NM_001382700.1:c.*998dup	NP_001369629.1:n.*998dup
NM_001382701.1:c.*998dup	NP_001369630.1:n.*998dup
NM_001382702.1:c.*998dup	NP_001369631.1:n.*998dup
NR_168483.1:n.3297dup