Canonical Allele Identifier: CA400555943

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61563984G>A (hg19) ; chr17:g.63486623G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486623G>A , CM000679.2:g.63486623G>A	GRCh38
NC_000017.10:g.61563984G>A , CM000679.1:g.61563984G>A	GRCh37
NC_000017.9:g.58917716G>A	NCBI36
NG_011648.1:g.14551G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2125G>A MANE Select	ENSP00000290866.4:p.Val709Met
ENST00000290863.10:c.403G>A	ENSP00000290863.6:p.Val135Met
ENST00000290866.9:c.2125G>A	ENSP00000290866.4:p.Val709Met
ENST00000413513.7:c.403G>A	ENSP00000392247.3:p.Val135Met
ENST00000428043.5:c.2125G>A	ENSP00000397593.2:p.Val709Met
ENST00000577647.2:c.403G>A	ENSP00000464149.1:p.Val135Met
ENST00000578839.5:c.*195G>A	ENSP00000462110.2:n.*195G>A
ENST00000579204.1:c.306G>A	ENSP00000464629.1:n.306G>A
ENST00000579314.5:c.403G>A	ENSP00000462599.1:p.Val135Met
ENST00000579726.5:c.687G>A
ENST00000582005.5:c.*45G>A	ENSP00000462002.1:n.*45G>A
NM_000789.3:c.2125G>A	NP_000780.1:p.Val709Met
NM_001178057.1:c.403G>A	NP_001171528.1:p.Val135Met
NM_152830.2:c.403G>A	NP_690043.1:p.Val135Met
XM_005257110.1:c.1576G>A	XP_005257167.1:p.Val526Met
XM_006721737.2:c.463G>A	XP_006721800.2:p.Val155Met
XM_006721737.3:c.463G>A	XP_006721800.2:p.Val155Met
NM_000789.4:c.2125G>A MANE Select	NP_000780.1:p.Val709Met
NM_001178057.2:c.403G>A	NP_001171528.1:p.Val135Met
NM_152830.3:c.403G>A	NP_690043.1:p.Val135Met
NM_001382700.1:c.1558G>A	NP_001369629.1:p.Val520Met
NM_001382701.1:c.1273G>A	NP_001369630.1:p.Val425Met
NM_001382702.1:c.55G>A	NP_001369631.1:p.Val19Met
NR_168483.1:n.425G>A