Canonical Allele Identifier: CA501184133

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61563968G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486607G>A , CM000679.2:g.63486607G>A	GRCh38
NC_000017.10:g.61563968G>A , CM000679.1:g.61563968G>A	GRCh37
NC_000017.9:g.58917700G>A	NCBI36
NG_011648.1:g.14535G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2109G>A MANE Select	ENSP00000290866.4:p.Gln703=
ENST00000290863.10:c.387G>A	ENSP00000290863.6:p.Gln129=
ENST00000290866.9:c.2109G>A	ENSP00000290866.4:p.Gln703=
ENST00000413513.7:c.387G>A	ENSP00000392247.3:p.Gln129=
ENST00000428043.5:c.2109G>A	ENSP00000397593.2:p.Gln703=
ENST00000577647.2:c.387G>A	ENSP00000464149.1:p.Gln129=
ENST00000578839.5:c.*179G>A	ENSP00000462110.2:n.*179G>A
ENST00000579204.1:c.290G>A	ENSP00000464629.1:n.290G>A
ENST00000579314.5:c.387G>A	ENSP00000462599.1:p.Gln129=
ENST00000579726.5:c.671G>A
ENST00000582005.5:c.*29G>A	ENSP00000462002.1:n.*29G>A
NM_000789.3:c.2109G>A	NP_000780.1:p.Gln703=
NM_001178057.1:c.387G>A	NP_001171528.1:p.Gln129=
NM_152830.2:c.387G>A	NP_690043.1:p.Gln129=
XM_005257110.1:c.1560G>A	XP_005257167.1:p.Gln520=
XM_006721737.2:c.447G>A	XP_006721800.2:p.Gln149=
XM_006721737.3:c.447G>A	XP_006721800.2:p.Gln149=
NM_000789.4:c.2109G>A MANE Select	NP_000780.1:p.Gln703=
NM_001178057.2:c.387G>A	NP_001171528.1:p.Gln129=
NM_152830.3:c.387G>A	NP_690043.1:p.Gln129=
NM_001382700.1:c.1542G>A	NP_001369629.1:p.Gln514=
NM_001382701.1:c.1257G>A	NP_001369630.1:p.Gln419=
NM_001382702.1:c.39G>A	NP_001369631.1:p.Gln13=
NR_168483.1:n.409G>A