Canonical Allele Identifier: CA501184148

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61563971C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486610C>G , CM000679.2:g.63486610C>G	GRCh38
NC_000017.10:g.61563971C>G , CM000679.1:g.61563971C>G	GRCh37
NC_000017.9:g.58917703C>G	NCBI36
NG_011648.1:g.14538C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2112C>G MANE Select	ENSP00000290866.4:p.Ala704=
ENST00000290863.10:c.390C>G	ENSP00000290863.6:p.Ala130=
ENST00000290866.9:c.2112C>G	ENSP00000290866.4:p.Ala704=
ENST00000413513.7:c.390C>G	ENSP00000392247.3:p.Ala130=
ENST00000428043.5:c.2112C>G	ENSP00000397593.2:p.Ala704=
ENST00000577647.2:c.390C>G	ENSP00000464149.1:p.Ala130=
ENST00000578839.5:c.*182C>G	ENSP00000462110.2:n.*182C>G
ENST00000579204.1:c.293C>G	ENSP00000464629.1:n.293C>G
ENST00000579314.5:c.390C>G	ENSP00000462599.1:p.Ala130=
ENST00000579726.5:c.674C>G
ENST00000582005.5:c.*32C>G	ENSP00000462002.1:n.*32C>G
NM_000789.3:c.2112C>G	NP_000780.1:p.Ala704=
NM_001178057.1:c.390C>G	NP_001171528.1:p.Ala130=
NM_152830.2:c.390C>G	NP_690043.1:p.Ala130=
XM_005257110.1:c.1563C>G	XP_005257167.1:p.Ala521=
XM_006721737.2:c.450C>G	XP_006721800.2:p.Ala150=
XM_006721737.3:c.450C>G	XP_006721800.2:p.Ala150=
NM_000789.4:c.2112C>G MANE Select	NP_000780.1:p.Ala704=
NM_001178057.2:c.390C>G	NP_001171528.1:p.Ala130=
NM_152830.3:c.390C>G	NP_690043.1:p.Ala130=
NM_001382700.1:c.1545C>G	NP_001369629.1:p.Ala515=
NM_001382701.1:c.1260C>G	NP_001369630.1:p.Ala420=
NM_001382702.1:c.42C>G	NP_001369631.1:p.Ala14=
NR_168483.1:n.412C>G