Canonical Allele Identifier: CA501187976

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566360A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488999A>G , CM000679.2:g.63488999A>G	GRCh38
NC_000017.10:g.61566360A>G , CM000679.1:g.61566360A>G	GRCh37
NC_000017.9:g.58920092A>G	NCBI36
NG_011648.1:g.16927A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2508A>G MANE Select	ENSP00000290866.4:p.Gln836=
ENST00000290863.10:c.786A>G	ENSP00000290863.6:p.Gln262=
ENST00000290866.9:c.2508A>G	ENSP00000290866.4:p.Gln836=
ENST00000413513.7:c.786A>G	ENSP00000392247.3:p.Gln262=
ENST00000428043.5:c.2508A>G	ENSP00000397593.2:p.Gln836=
ENST00000577647.2:c.786A>G	ENSP00000464149.1:p.Gln262=
ENST00000578839.5:c.*519+208A>G	ENSP00000462110.2:n.*519+208A>G
ENST00000579204.1:c.767A>G	ENSP00000464629.1:n.767A>G
ENST00000579314.5:c.*237A>G	ENSP00000462599.1:n.*237A>G
ENST00000582005.5:c.*428A>G	ENSP00000462002.1:n.*428A>G
ENST00000582761.1:c.276A>G	ENSP00000462909.1:p.Gln92=
ENST00000584865.5:n.454A>G
NM_000789.3:c.2508A>G	NP_000780.1:p.Gln836=
NM_001178057.1:c.786A>G	NP_001171528.1:p.Gln262=
NM_152830.2:c.786A>G	NP_690043.1:p.Gln262=
XM_005257110.1:c.1959A>G	XP_005257167.1:p.Gln653=
XM_006721737.2:c.846A>G	XP_006721800.2:p.Gln282=
XM_006721737.3:c.846A>G	XP_006721800.2:p.Gln282=
NM_000789.4:c.2508A>G MANE Select	NP_000780.1:p.Gln836=
NM_001178057.2:c.786A>G	NP_001171528.1:p.Gln262=
NM_152830.3:c.786A>G	NP_690043.1:p.Gln262=
NM_001382700.1:c.1941A>G	NP_001369629.1:p.Gln647=
NM_001382701.1:c.1656A>G	NP_001369630.1:p.Gln552=
NM_001382702.1:c.379+208A>G	NP_001369631.1:n.379+208A>G
NR_168483.1:n.886A>G