Canonical Allele Identifier: CA400567417

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574272A>G (hg19) ; chr17:g.63496911A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496911A>G , CM000679.2:g.63496911A>G	GRCh38
NC_000017.10:g.61574272A>G , CM000679.1:g.61574272A>G	GRCh37
NC_000017.9:g.58928004A>G	NCBI36
NG_011648.1:g.24839A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3617A>G MANE Select	ENSP00000290866.4:p.Asp1206Gly
ENST00000290863.10:c.1895A>G	ENSP00000290863.6:p.Asp632Gly
ENST00000290866.9:c.3617A>G	ENSP00000290866.4:p.Asp1206Gly
ENST00000413513.7:c.1772A>G	ENSP00000392247.3:p.Asp591Gly
ENST00000428043.5:c.3617A>G	ENSP00000397593.2:p.Asp1206Gly
ENST00000577418.5:n.627A>G
ENST00000577647.2:c.1895A>G	ENSP00000464149.1:p.Asp632Gly
ENST00000578839.5:c.*1372A>G	ENSP00000462110.2:n.*1372A>G
ENST00000579314.5:c.*1346A>G	ENSP00000462599.1:n.*1346A>G
ENST00000579409.1:c.304A>G
ENST00000582244.1:n.491A>G
NM_000789.3:c.3617A>G	NP_000780.1:p.Asp1206Gly
NM_001178057.1:c.1772A>G	NP_001171528.1:p.Asp591Gly
NM_152830.2:c.1895A>G	NP_690043.1:p.Asp632Gly
XM_005257110.1:c.3068A>G	XP_005257167.1:p.Asp1023Gly
XM_006721737.2:c.1955A>G	XP_006721800.2:p.Asp652Gly
XM_006721737.3:c.1955A>G	XP_006721800.2:p.Asp652Gly
NM_000789.4:c.3617A>G MANE Select	NP_000780.1:p.Asp1206Gly
NM_001178057.2:c.1772A>G	NP_001171528.1:p.Asp591Gly
NM_152830.3:c.1895A>G	NP_690043.1:p.Asp632Gly
NM_001382700.1:c.3050A>G	NP_001369629.1:p.Asp1017Gly
NM_001382701.1:c.2765A>G	NP_001369630.1:p.Asp922Gly
NM_001382702.1:c.1232A>G	NP_001369631.1:p.Asp411Gly
NR_168483.1:n.1995A>G