Canonical Allele Identifier: CA400566758

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574197A>G (hg19) ; chr17:g.63496836A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496836A>G , CM000679.2:g.63496836A>G	GRCh38
NC_000017.10:g.61574197A>G , CM000679.1:g.61574197A>G	GRCh37
NC_000017.9:g.58927929A>G	NCBI36
NG_011648.1:g.24764A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3542A>G MANE Select	ENSP00000290866.4:p.Glu1181Gly
ENST00000290863.10:c.1820A>G	ENSP00000290863.6:p.Glu607Gly
ENST00000290866.9:c.3542A>G	ENSP00000290866.4:p.Glu1181Gly
ENST00000413513.7:c.1697A>G	ENSP00000392247.3:p.Glu566Gly
ENST00000428043.5:c.3542A>G	ENSP00000397593.2:p.Glu1181Gly
ENST00000577418.5:n.552A>G
ENST00000577647.2:c.1820A>G	ENSP00000464149.1:p.Glu607Gly
ENST00000578839.5:c.*1297A>G	ENSP00000462110.2:n.*1297A>G
ENST00000579314.5:c.*1271A>G	ENSP00000462599.1:n.*1271A>G
ENST00000579409.1:c.229A>G
ENST00000582244.1:n.416A>G
NM_000789.3:c.3542A>G	NP_000780.1:p.Glu1181Gly
NM_001178057.1:c.1697A>G	NP_001171528.1:p.Glu566Gly
NM_152830.2:c.1820A>G	NP_690043.1:p.Glu607Gly
XM_005257110.1:c.2993A>G	XP_005257167.1:p.Glu998Gly
XM_006721737.2:c.1880A>G	XP_006721800.2:p.Glu627Gly
XM_006721737.3:c.1880A>G	XP_006721800.2:p.Glu627Gly
NM_000789.4:c.3542A>G MANE Select	NP_000780.1:p.Glu1181Gly
NM_001178057.2:c.1697A>G	NP_001171528.1:p.Glu566Gly
NM_152830.3:c.1820A>G	NP_690043.1:p.Glu607Gly
NM_001382700.1:c.2975A>G	NP_001369629.1:p.Glu992Gly
NM_001382701.1:c.2690A>G	NP_001369630.1:p.Glu897Gly
NM_001382702.1:c.1157A>G	NP_001369631.1:p.Glu386Gly
NR_168483.1:n.1920A>G