Canonical Allele Identifier: CA400568428

Gene: ACE

Linked Data

• gnomAD v4: 17-63497169-C-A
• MyVariant Identifiers: chr17:g.61574530C>A (hg19) ; chr17:g.63497169C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497169C>A , CM000679.2:g.63497169C>A	GRCh38
NC_000017.10:g.61574530C>A , CM000679.1:g.61574530C>A	GRCh37
NC_000017.9:g.58928262C>A	NCBI36
NG_011648.1:g.25097C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3724C>A MANE Select	ENSP00000290866.4:p.Arg1242Ser
ENST00000290863.10:c.2002C>A	ENSP00000290863.6:p.Arg668Ser
ENST00000290866.9:c.3724C>A	ENSP00000290866.4:p.Arg1242Ser
ENST00000413513.7:c.1879C>A	ENSP00000392247.3:p.Arg627Ser
ENST00000428043.5:c.*146C>A	ENSP00000397593.2:n.*146C>A
ENST00000577647.2:c.1969+184C>A	ENSP00000464149.1:n.1969+184C>A
ENST00000578839.5:c.*1479C>A	ENSP00000462110.2:n.*1479C>A
ENST00000579314.5:c.*1453C>A	ENSP00000462599.1:n.*1453C>A
NM_000789.3:c.3724C>A	NP_000780.1:p.Arg1242Ser
NM_001178057.1:c.1879C>A	NP_001171528.1:p.Arg627Ser
NM_152830.2:c.2002C>A	NP_690043.1:p.Arg668Ser
XM_005257110.1:c.3175C>A	XP_005257167.1:p.Arg1059Ser
XM_006721737.2:c.2062C>A	XP_006721800.2:p.Arg688Ser
XM_006721737.3:c.2062C>A	XP_006721800.2:p.Arg688Ser
NM_000789.4:c.3724C>A MANE Select	NP_000780.1:p.Arg1242Ser
NM_001178057.2:c.1879C>A	NP_001171528.1:p.Arg627Ser
NM_152830.3:c.2002C>A	NP_690043.1:p.Arg668Ser
NM_001382700.1:c.3157C>A	NP_001369629.1:p.Arg1053Ser
NM_001382701.1:c.2872C>A	NP_001369630.1:p.Arg958Ser
NM_001382702.1:c.1339C>A	NP_001369631.1:p.Arg447Ser
NR_168483.1:n.2102C>A