Canonical Allele Identifier: CA400568968

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574612T>G (hg19) ; chr17:g.63497251T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497251T>G , CM000679.2:g.63497251T>G	GRCh38
NC_000017.10:g.61574612T>G , CM000679.1:g.61574612T>G	GRCh37
NC_000017.9:g.58928344T>G	NCBI36
NG_011648.1:g.25179T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3806T>G MANE Select	ENSP00000290866.4:p.Leu1269Arg
ENST00000290863.10:c.2084T>G	ENSP00000290863.6:p.Leu695Arg
ENST00000290866.9:c.3806T>G	ENSP00000290866.4:p.Leu1269Arg
ENST00000413513.7:c.1961T>G	ENSP00000392247.3:p.Leu654Arg
ENST00000428043.5:c.*228T>G	ENSP00000397593.2:n.*228T>G
ENST00000577647.2:c.1969+266T>G	ENSP00000464149.1:n.1969+266T>G
ENST00000578839.5:c.*1561T>G	ENSP00000462110.2:n.*1561T>G
ENST00000579314.5:c.*1535T>G	ENSP00000462599.1:n.*1535T>G
NM_000789.3:c.3806T>G	NP_000780.1:p.Leu1269Arg
NM_001178057.1:c.1961T>G	NP_001171528.1:p.Leu654Arg
NM_152830.2:c.2084T>G	NP_690043.1:p.Leu695Arg
XM_005257110.1:c.3257T>G	XP_005257167.1:p.Leu1086Arg
XM_006721737.2:c.2144T>G	XP_006721800.2:p.Leu715Arg
XM_006721737.3:c.2144T>G	XP_006721800.2:p.Leu715Arg
NM_000789.4:c.3806T>G MANE Select	NP_000780.1:p.Leu1269Arg
NM_001178057.2:c.1961T>G	NP_001171528.1:p.Leu654Arg
NM_152830.3:c.2084T>G	NP_690043.1:p.Leu695Arg
NM_001382700.1:c.3239T>G	NP_001369629.1:p.Leu1080Arg
NM_001382701.1:c.2954T>G	NP_001369630.1:p.Leu985Arg
NM_001382702.1:c.1421T>G	NP_001369631.1:p.Leu474Arg
NR_168483.1:n.2184T>G