Canonical Allele Identifier: CA501342310

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574201C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496840C>A , CM000679.2:g.63496840C>A	GRCh38
NC_000017.10:g.61574201C>A , CM000679.1:g.61574201C>A	GRCh37
NC_000017.9:g.58927933C>A	NCBI36
NG_011648.1:g.24768C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3546C>A MANE Select	ENSP00000290866.4:p.Ala1182=
ENST00000290863.10:c.1824C>A	ENSP00000290863.6:p.Ala608=
ENST00000290866.9:c.3546C>A	ENSP00000290866.4:p.Ala1182=
ENST00000413513.7:c.1701C>A	ENSP00000392247.3:p.Ala567=
ENST00000428043.5:c.3546C>A	ENSP00000397593.2:p.Ala1182=
ENST00000577418.5:n.556C>A
ENST00000577647.2:c.1824C>A	ENSP00000464149.1:p.Ala608=
ENST00000578839.5:c.*1301C>A	ENSP00000462110.2:n.*1301C>A
ENST00000579314.5:c.*1275C>A	ENSP00000462599.1:n.*1275C>A
ENST00000579409.1:c.233C>A
ENST00000582244.1:n.420C>A
NM_000789.3:c.3546C>A	NP_000780.1:p.Ala1182=
NM_001178057.1:c.1701C>A	NP_001171528.1:p.Ala567=
NM_152830.2:c.1824C>A	NP_690043.1:p.Ala608=
XM_005257110.1:c.2997C>A	XP_005257167.1:p.Ala999=
XM_006721737.2:c.1884C>A	XP_006721800.2:p.Ala628=
XM_006721737.3:c.1884C>A	XP_006721800.2:p.Ala628=
NM_000789.4:c.3546C>A MANE Select	NP_000780.1:p.Ala1182=
NM_001178057.2:c.1701C>A	NP_001171528.1:p.Ala567=
NM_152830.3:c.1824C>A	NP_690043.1:p.Ala608=
NM_001382700.1:c.2979C>A	NP_001369629.1:p.Ala993=
NM_001382701.1:c.2694C>A	NP_001369630.1:p.Ala898=
NM_001382702.1:c.1161C>A	NP_001369631.1:p.Ala387=
NR_168483.1:n.1924C>A