Canonical Allele Identifier: CA400569452

Gene: ACE

Linked Data

• gnomAD v4: 17-63497312-C-A
• MyVariant Identifiers: chr17:g.61574673C>A (hg19) ; chr17:g.63497312C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497312C>A , CM000679.2:g.63497312C>A	GRCh38
NC_000017.10:g.61574673C>A , CM000679.1:g.61574673C>A	GRCh37
NC_000017.9:g.58928405C>A	NCBI36
NG_011648.1:g.25240C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3867C>A MANE Select	ENSP00000290866.4:p.His1289Gln
ENST00000290863.10:c.2145C>A	ENSP00000290863.6:p.His715Gln
ENST00000290866.9:c.3867C>A	ENSP00000290866.4:p.His1289Gln
ENST00000413513.7:c.2022C>A	ENSP00000392247.3:p.His674Gln
ENST00000428043.5:c.*289C>A	ENSP00000397593.2:n.*289C>A
ENST00000577647.2:c.1969+327C>A	ENSP00000464149.1:n.1969+327C>A
ENST00000578839.5:c.*1622C>A	ENSP00000462110.2:n.*1622C>A
ENST00000579314.5:c.*1596C>A	ENSP00000462599.1:n.*1596C>A
NM_000789.3:c.3867C>A	NP_000780.1:p.His1289Gln
NM_001178057.1:c.2022C>A	NP_001171528.1:p.His674Gln
NM_152830.2:c.2145C>A	NP_690043.1:p.His715Gln
XM_005257110.1:c.3318C>A	XP_005257167.1:p.His1106Gln
XM_006721737.2:c.2205C>A	XP_006721800.2:p.His735Gln
XM_006721737.3:c.2205C>A	XP_006721800.2:p.His735Gln
NM_000789.4:c.3867C>A MANE Select	NP_000780.1:p.His1289Gln
NM_001178057.2:c.2022C>A	NP_001171528.1:p.His674Gln
NM_152830.3:c.2145C>A	NP_690043.1:p.His715Gln
NM_001382700.1:c.3300C>A	NP_001369629.1:p.His1100Gln
NM_001382701.1:c.3015C>A	NP_001369630.1:p.His1005Gln
NM_001382702.1:c.1482C>A	NP_001369631.1:p.His494Gln
NR_168483.1:n.2245C>A