Canonical Allele Identifier: CA400556039

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61563999A>C (hg19) ; chr17:g.63486638A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486638A>C , CM000679.2:g.63486638A>C	GRCh38
NC_000017.10:g.61563999A>C , CM000679.1:g.61563999A>C	GRCh37
NC_000017.9:g.58917731A>C	NCBI36
NG_011648.1:g.14566A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2140A>C MANE Select	ENSP00000290866.4:p.Asn714His
ENST00000290863.10:c.418A>C	ENSP00000290863.6:p.Asn140His
ENST00000290866.9:c.2140A>C	ENSP00000290866.4:p.Asn714His
ENST00000413513.7:c.418A>C	ENSP00000392247.3:p.Asn140His
ENST00000428043.5:c.2140A>C	ENSP00000397593.2:p.Asn714His
ENST00000577647.2:c.418A>C	ENSP00000464149.1:p.Asn140His
ENST00000578839.5:c.*210A>C	ENSP00000462110.2:n.*210A>C
ENST00000579204.1:c.321A>C	ENSP00000464629.1:n.321A>C
ENST00000579314.5:c.418A>C	ENSP00000462599.1:p.Asn140His
ENST00000579726.5:c.702A>C
ENST00000582005.5:c.*60A>C	ENSP00000462002.1:n.*60A>C
NM_000789.3:c.2140A>C	NP_000780.1:p.Asn714His
NM_001178057.1:c.418A>C	NP_001171528.1:p.Asn140His
NM_152830.2:c.418A>C	NP_690043.1:p.Asn140His
XM_005257110.1:c.1591A>C	XP_005257167.1:p.Asn531His
XM_006721737.2:c.478A>C	XP_006721800.2:p.Asn160His
XM_006721737.3:c.478A>C	XP_006721800.2:p.Asn160His
NM_000789.4:c.2140A>C MANE Select	NP_000780.1:p.Asn714His
NM_001178057.2:c.418A>C	NP_001171528.1:p.Asn140His
NM_152830.3:c.418A>C	NP_690043.1:p.Asn140His
NM_001382700.1:c.1573A>C	NP_001369629.1:p.Asn525His
NM_001382701.1:c.1288A>C	NP_001369630.1:p.Asn430His
NM_001382702.1:c.70A>C	NP_001369631.1:p.Asn24His
NR_168483.1:n.440A>C