Canonical Allele Identifier: CA400556400

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61564073G>C (hg19) ; chr17:g.63486712G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486712G>C , CM000679.2:g.63486712G>C	GRCh38
NC_000017.10:g.61564073G>C , CM000679.1:g.61564073G>C	GRCh37
NC_000017.9:g.58917805G>C	NCBI36
NG_011648.1:g.14640G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2214G>C MANE Select	ENSP00000290866.4:p.Glu738Asp
ENST00000290863.10:c.492G>C	ENSP00000290863.6:p.Glu164Asp
ENST00000290866.9:c.2214G>C	ENSP00000290866.4:p.Glu738Asp
ENST00000413513.7:c.492G>C	ENSP00000392247.3:p.Glu164Asp
ENST00000428043.5:c.2214G>C	ENSP00000397593.2:p.Glu738Asp
ENST00000577647.2:c.492G>C	ENSP00000464149.1:p.Glu164Asp
ENST00000578839.5:c.*284G>C	ENSP00000462110.2:n.*284G>C
ENST00000579204.1:c.395G>C	ENSP00000464629.1:n.395G>C
ENST00000579314.5:c.492G>C	ENSP00000462599.1:p.Glu164Asp
ENST00000579726.5:c.776G>C
ENST00000582005.5:c.*134G>C	ENSP00000462002.1:n.*134G>C
NM_000789.3:c.2214G>C	NP_000780.1:p.Glu738Asp
NM_001178057.1:c.492G>C	NP_001171528.1:p.Glu164Asp
NM_152830.2:c.492G>C	NP_690043.1:p.Glu164Asp
XM_005257110.1:c.1665G>C	XP_005257167.1:p.Glu555Asp
XM_006721737.2:c.552G>C	XP_006721800.2:p.Glu184Asp
XM_006721737.3:c.552G>C	XP_006721800.2:p.Glu184Asp
NM_000789.4:c.2214G>C MANE Select	NP_000780.1:p.Glu738Asp
NM_001178057.2:c.492G>C	NP_001171528.1:p.Glu164Asp
NM_152830.3:c.492G>C	NP_690043.1:p.Glu164Asp
NM_001382700.1:c.1647G>C	NP_001369629.1:p.Glu549Asp
NM_001382701.1:c.1362G>C	NP_001369630.1:p.Glu454Asp
NM_001382702.1:c.144G>C	NP_001369631.1:p.Glu48Asp
NR_168483.1:n.514G>C