Canonical Allele Identifier: CA400569118

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574638C>G (hg19) ; chr17:g.63497277C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497277C>G , CM000679.2:g.63497277C>G	GRCh38
NC_000017.10:g.61574638C>G , CM000679.1:g.61574638C>G	GRCh37
NC_000017.9:g.58928370C>G	NCBI36
NG_011648.1:g.25205C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3832C>G MANE Select	ENSP00000290866.4:p.Gln1278Glu
ENST00000290863.10:c.2110C>G	ENSP00000290863.6:p.Gln704Glu
ENST00000290866.9:c.3832C>G	ENSP00000290866.4:p.Gln1278Glu
ENST00000413513.7:c.1987C>G	ENSP00000392247.3:p.Gln663Glu
ENST00000428043.5:c.*254C>G	ENSP00000397593.2:n.*254C>G
ENST00000577647.2:c.1969+292C>G	ENSP00000464149.1:n.1969+292C>G
ENST00000578839.5:c.*1587C>G	ENSP00000462110.2:n.*1587C>G
ENST00000579314.5:c.*1561C>G	ENSP00000462599.1:n.*1561C>G
NM_000789.3:c.3832C>G	NP_000780.1:p.Gln1278Glu
NM_001178057.1:c.1987C>G	NP_001171528.1:p.Gln663Glu
NM_152830.2:c.2110C>G	NP_690043.1:p.Gln704Glu
XM_005257110.1:c.3283C>G	XP_005257167.1:p.Gln1095Glu
XM_006721737.2:c.2170C>G	XP_006721800.2:p.Gln724Glu
XM_006721737.3:c.2170C>G	XP_006721800.2:p.Gln724Glu
NM_000789.4:c.3832C>G MANE Select	NP_000780.1:p.Gln1278Glu
NM_001178057.2:c.1987C>G	NP_001171528.1:p.Gln663Glu
NM_152830.3:c.2110C>G	NP_690043.1:p.Gln704Glu
NM_001382700.1:c.3265C>G	NP_001369629.1:p.Gln1089Glu
NM_001382701.1:c.2980C>G	NP_001369630.1:p.Gln994Glu
NM_001382702.1:c.1447C>G	NP_001369631.1:p.Gln483Glu
NR_168483.1:n.2210C>G