Canonical Allele Identifier: CA501186835

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566046A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488685A>G , CM000679.2:g.63488685A>G	GRCh38
NC_000017.10:g.61566046A>G , CM000679.1:g.61566046A>G	GRCh37
NC_000017.9:g.58919778A>G	NCBI36
NG_011648.1:g.16613A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.2343A>G MANE Select	ENSP00000290866.4:p.Glu781=
ENST00000290863.10:c.621A>G	ENSP00000290863.6:p.Glu207=
ENST00000290866.9:c.2343A>G	ENSP00000290866.4:p.Glu781=
ENST00000413513.7:c.621A>G	ENSP00000392247.3:p.Glu207=
ENST00000428043.5:c.2343A>G	ENSP00000397593.2:p.Glu781=
ENST00000577647.2:c.621A>G	ENSP00000464149.1:p.Glu207=
ENST00000578839.5:c.*413A>G	ENSP00000462110.2:n.*413A>G
ENST00000579204.1:c.602A>G	ENSP00000464629.1:n.602A>G
ENST00000579314.5:c.*72A>G	ENSP00000462599.1:n.*72A>G
ENST00000582005.5:c.*263A>G	ENSP00000462002.1:n.*263A>G
ENST00000582761.1:c.111A>G	ENSP00000462909.1:p.Glu37=
ENST00000584865.5:n.289A>G
NM_000789.3:c.2343A>G	NP_000780.1:p.Glu781=
NM_001178057.1:c.621A>G	NP_001171528.1:p.Glu207=
NM_152830.2:c.621A>G	NP_690043.1:p.Glu207=
XM_005257110.1:c.1794A>G	XP_005257167.1:p.Glu598=
XM_006721737.2:c.681A>G	XP_006721800.2:p.Glu227=
XM_006721737.3:c.681A>G	XP_006721800.2:p.Glu227=
NM_000789.4:c.2343A>G MANE Select	NP_000780.1:p.Glu781=
NM_001178057.2:c.621A>G	NP_001171528.1:p.Glu207=
NM_152830.3:c.621A>G	NP_690043.1:p.Glu207=
NM_001382700.1:c.1776A>G	NP_001369629.1:p.Glu592=
NM_001382701.1:c.1491A>G	NP_001369630.1:p.Glu497=
NM_001382702.1:c.273A>G	NP_001369631.1:p.Glu91=
NR_168483.1:n.721A>G