Canonical Allele Identifier: CA501342339

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574580C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497219C>G , CM000679.2:g.63497219C>G	GRCh38
NC_000017.10:g.61574580C>G , CM000679.1:g.61574580C>G	GRCh37
NC_000017.9:g.58928312C>G	NCBI36
NG_011648.1:g.25147C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3774C>G MANE Select	ENSP00000290866.4:p.Gly1258=
ENST00000290863.10:c.2052C>G	ENSP00000290863.6:p.Gly684=
ENST00000290866.9:c.3774C>G	ENSP00000290866.4:p.Gly1258=
ENST00000413513.7:c.1929C>G	ENSP00000392247.3:p.Gly643=
ENST00000428043.5:c.*196C>G	ENSP00000397593.2:n.*196C>G
ENST00000577647.2:c.1969+234C>G	ENSP00000464149.1:n.1969+234C>G
ENST00000578839.5:c.*1529C>G	ENSP00000462110.2:n.*1529C>G
ENST00000579314.5:c.*1503C>G	ENSP00000462599.1:n.*1503C>G
NM_000789.3:c.3774C>G	NP_000780.1:p.Gly1258=
NM_001178057.1:c.1929C>G	NP_001171528.1:p.Gly643=
NM_152830.2:c.2052C>G	NP_690043.1:p.Gly684=
XM_005257110.1:c.3225C>G	XP_005257167.1:p.Gly1075=
XM_006721737.2:c.2112C>G	XP_006721800.2:p.Gly704=
XM_006721737.3:c.2112C>G	XP_006721800.2:p.Gly704=
NM_000789.4:c.3774C>G MANE Select	NP_000780.1:p.Gly1258=
NM_001178057.2:c.1929C>G	NP_001171528.1:p.Gly643=
NM_152830.3:c.2052C>G	NP_690043.1:p.Gly684=
NM_001382700.1:c.3207C>G	NP_001369629.1:p.Gly1069=
NM_001382701.1:c.2922C>G	NP_001369630.1:p.Gly974=
NM_001382702.1:c.1389C>G	NP_001369631.1:p.Gly463=
NR_168483.1:n.2152C>G