Canonical Allele Identifier: CA400568586

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574552A>T (hg19) ; chr17:g.63497191A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497191A>T , CM000679.2:g.63497191A>T	GRCh38
NC_000017.10:g.61574552A>T , CM000679.1:g.61574552A>T	GRCh37
NC_000017.9:g.58928284A>T	NCBI36
NG_011648.1:g.25119A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3746A>T MANE Select	ENSP00000290866.4:p.Asp1249Val
ENST00000290863.10:c.2024A>T	ENSP00000290863.6:p.Asp675Val
ENST00000290866.9:c.3746A>T	ENSP00000290866.4:p.Asp1249Val
ENST00000413513.7:c.1901A>T	ENSP00000392247.3:p.Asp634Val
ENST00000428043.5:c.*168A>T	ENSP00000397593.2:n.*168A>T
ENST00000577647.2:c.1969+206A>T	ENSP00000464149.1:n.1969+206A>T
ENST00000578839.5:c.*1501A>T	ENSP00000462110.2:n.*1501A>T
ENST00000579314.5:c.*1475A>T	ENSP00000462599.1:n.*1475A>T
NM_000789.3:c.3746A>T	NP_000780.1:p.Asp1249Val
NM_001178057.1:c.1901A>T	NP_001171528.1:p.Asp634Val
NM_152830.2:c.2024A>T	NP_690043.1:p.Asp675Val
XM_005257110.1:c.3197A>T	XP_005257167.1:p.Asp1066Val
XM_006721737.2:c.2084A>T	XP_006721800.2:p.Asp695Val
XM_006721737.3:c.2084A>T	XP_006721800.2:p.Asp695Val
NM_000789.4:c.3746A>T MANE Select	NP_000780.1:p.Asp1249Val
NM_001178057.2:c.1901A>T	NP_001171528.1:p.Asp634Val
NM_152830.3:c.2024A>T	NP_690043.1:p.Asp675Val
NM_001382700.1:c.3179A>T	NP_001369629.1:p.Asp1060Val
NM_001382701.1:c.2894A>T	NP_001369630.1:p.Asp965Val
NM_001382702.1:c.1361A>T	NP_001369631.1:p.Asp454Val
NR_168483.1:n.2124A>T