Canonical Allele Identifier: CA400568796

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574584T>A (hg19) ; chr17:g.63497223T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497223T>A , CM000679.2:g.63497223T>A	GRCh38
NC_000017.10:g.61574584T>A , CM000679.1:g.61574584T>A	GRCh37
NC_000017.9:g.58928316T>A	NCBI36
NG_011648.1:g.25151T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3778T>A MANE Select	ENSP00000290866.4:p.Trp1260Arg
ENST00000290863.10:c.2056T>A	ENSP00000290863.6:p.Trp686Arg
ENST00000290866.9:c.3778T>A	ENSP00000290866.4:p.Trp1260Arg
ENST00000413513.7:c.1933T>A	ENSP00000392247.3:p.Trp645Arg
ENST00000428043.5:c.*200T>A	ENSP00000397593.2:n.*200T>A
ENST00000577647.2:c.1969+238T>A	ENSP00000464149.1:n.1969+238T>A
ENST00000578839.5:c.*1533T>A	ENSP00000462110.2:n.*1533T>A
ENST00000579314.5:c.*1507T>A	ENSP00000462599.1:n.*1507T>A
NM_000789.3:c.3778T>A	NP_000780.1:p.Trp1260Arg
NM_001178057.1:c.1933T>A	NP_001171528.1:p.Trp645Arg
NM_152830.2:c.2056T>A	NP_690043.1:p.Trp686Arg
XM_005257110.1:c.3229T>A	XP_005257167.1:p.Trp1077Arg
XM_006721737.2:c.2116T>A	XP_006721800.2:p.Trp706Arg
XM_006721737.3:c.2116T>A	XP_006721800.2:p.Trp706Arg
NM_000789.4:c.3778T>A MANE Select	NP_000780.1:p.Trp1260Arg
NM_001178057.2:c.1933T>A	NP_001171528.1:p.Trp645Arg
NM_152830.3:c.2056T>A	NP_690043.1:p.Trp686Arg
NM_001382700.1:c.3211T>A	NP_001369629.1:p.Trp1071Arg
NM_001382701.1:c.2926T>A	NP_001369630.1:p.Trp976Arg
NM_001382702.1:c.1393T>A	NP_001369631.1:p.Trp465Arg
NR_168483.1:n.2156T>A