Canonical Allele Identifier: CA400567688

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574314G>A (hg19) ; chr17:g.63496953G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496953G>A , CM000679.2:g.63496953G>A	GRCh38
NC_000017.10:g.61574314G>A , CM000679.1:g.61574314G>A	GRCh37
NC_000017.9:g.58928046G>A	NCBI36
NG_011648.1:g.24881G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3659G>A MANE Select	ENSP00000290866.4:p.Gly1220Asp
ENST00000290863.10:c.1937G>A	ENSP00000290863.6:p.Gly646Asp
ENST00000290866.9:c.3659G>A	ENSP00000290866.4:p.Gly1220Asp
ENST00000413513.7:c.1814G>A	ENSP00000392247.3:p.Gly605Asp
ENST00000428043.5:c.3659G>A	ENSP00000397593.2:p.Gly1220Asp
ENST00000577418.5:n.669G>A
ENST00000577647.2:c.1937G>A	ENSP00000464149.1:p.Gly646Asp
ENST00000578839.5:c.*1414G>A	ENSP00000462110.2:n.*1414G>A
ENST00000579314.5:c.*1388G>A	ENSP00000462599.1:n.*1388G>A
ENST00000579409.1:c.346G>A
ENST00000582244.1:n.533G>A
NM_000789.3:c.3659G>A	NP_000780.1:p.Gly1220Asp
NM_001178057.1:c.1814G>A	NP_001171528.1:p.Gly605Asp
NM_152830.2:c.1937G>A	NP_690043.1:p.Gly646Asp
XM_005257110.1:c.3110G>A	XP_005257167.1:p.Gly1037Asp
XM_006721737.2:c.1997G>A	XP_006721800.2:p.Gly666Asp
XM_006721737.3:c.1997G>A	XP_006721800.2:p.Gly666Asp
NM_000789.4:c.3659G>A MANE Select	NP_000780.1:p.Gly1220Asp
NM_001178057.2:c.1814G>A	NP_001171528.1:p.Gly605Asp
NM_152830.3:c.1937G>A	NP_690043.1:p.Gly646Asp
NM_001382700.1:c.3092G>A	NP_001369629.1:p.Gly1031Asp
NM_001382701.1:c.2807G>A	NP_001369630.1:p.Gly936Asp
NM_001382702.1:c.1274G>A	NP_001369631.1:p.Gly425Asp
NR_168483.1:n.2037G>A