Canonical Allele Identifier: CA501187948

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566309A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488948A>G , CM000679.2:g.63488948A>G	GRCh38
NC_000017.10:g.61566309A>G , CM000679.1:g.61566309A>G	GRCh37
NC_000017.9:g.58920041A>G	NCBI36
NG_011648.1:g.16876A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2457A>G MANE Select	ENSP00000290866.4:p.Val819=
ENST00000290863.10:c.735A>G	ENSP00000290863.6:p.Val245=
ENST00000290866.9:c.2457A>G	ENSP00000290866.4:p.Val819=
ENST00000413513.7:c.735A>G	ENSP00000392247.3:p.Val245=
ENST00000428043.5:c.2457A>G	ENSP00000397593.2:p.Val819=
ENST00000577647.2:c.735A>G	ENSP00000464149.1:p.Val245=
ENST00000578839.5:c.*519+157A>G	ENSP00000462110.2:n.*519+157A>G
ENST00000579204.1:c.716A>G	ENSP00000464629.1:n.716A>G
ENST00000579314.5:c.*186A>G	ENSP00000462599.1:n.*186A>G
ENST00000582005.5:c.*377A>G	ENSP00000462002.1:n.*377A>G
ENST00000582761.1:c.225A>G	ENSP00000462909.1:p.Val75=
ENST00000584865.5:n.403A>G
NM_000789.3:c.2457A>G	NP_000780.1:p.Val819=
NM_001178057.1:c.735A>G	NP_001171528.1:p.Val245=
NM_152830.2:c.735A>G	NP_690043.1:p.Val245=
XM_005257110.1:c.1908A>G	XP_005257167.1:p.Val636=
XM_006721737.2:c.795A>G	XP_006721800.2:p.Val265=
XM_006721737.3:c.795A>G	XP_006721800.2:p.Val265=
NM_000789.4:c.2457A>G MANE Select	NP_000780.1:p.Val819=
NM_001178057.2:c.735A>G	NP_001171528.1:p.Val245=
NM_152830.3:c.735A>G	NP_690043.1:p.Val245=
NM_001382700.1:c.1890A>G	NP_001369629.1:p.Val630=
NM_001382701.1:c.1605A>G	NP_001369630.1:p.Val535=
NM_001382702.1:c.379+157A>G	NP_001369631.1:n.379+157A>G
NR_168483.1:n.835A>G