Canonical Allele Identifier: CA400569482

Gene: ACE

Linked Data

• gnomAD v4: 17-63497316-C-T
• COSMIC: COSM6418455 ; COSM6418456
• MyVariant Identifiers: chr17:g.61574677C>T (hg19) ; chr17:g.63497316C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497316C>T , CM000679.2:g.63497316C>T	GRCh38
NC_000017.10:g.61574677C>T , CM000679.1:g.61574677C>T	GRCh37
NC_000017.9:g.58928409C>T	NCBI36
NG_011648.1:g.25244C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3871C>T MANE Select	ENSP00000290866.4:p.His1291Tyr
ENST00000290863.10:c.2149C>T	ENSP00000290863.6:p.His717Tyr
ENST00000290866.9:c.3871C>T	ENSP00000290866.4:p.His1291Tyr
ENST00000413513.7:c.2026C>T	ENSP00000392247.3:p.His676Tyr
ENST00000428043.5:c.*293C>T	ENSP00000397593.2:n.*293C>T
ENST00000577647.2:c.1969+331C>T	ENSP00000464149.1:n.1969+331C>T
ENST00000578839.5:c.*1626C>T	ENSP00000462110.2:n.*1626C>T
ENST00000579314.5:c.*1600C>T	ENSP00000462599.1:n.*1600C>T
NM_000789.3:c.3871C>T	NP_000780.1:p.His1291Tyr
NM_001178057.1:c.2026C>T	NP_001171528.1:p.His676Tyr
NM_152830.2:c.2149C>T	NP_690043.1:p.His717Tyr
XM_005257110.1:c.3322C>T	XP_005257167.1:p.His1108Tyr
XM_006721737.2:c.2209C>T	XP_006721800.2:p.His737Tyr
XM_006721737.3:c.2209C>T	XP_006721800.2:p.His737Tyr
NM_000789.4:c.3871C>T MANE Select	NP_000780.1:p.His1291Tyr
NM_001178057.2:c.2026C>T	NP_001171528.1:p.His676Tyr
NM_152830.3:c.2149C>T	NP_690043.1:p.His717Tyr
NM_001382700.1:c.3304C>T	NP_001369629.1:p.His1102Tyr
NM_001382701.1:c.3019C>T	NP_001369630.1:p.His1007Tyr
NM_001382702.1:c.1486C>T	NP_001369631.1:p.His496Tyr
NR_168483.1:n.2249C>T