Canonical Allele Identifier: CA400549161

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61559874A>G (hg19) ; chr17:g.63482513A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63482513A>G , CM000679.2:g.63482513A>G	GRCh38
NC_000017.10:g.61559874A>G , CM000679.1:g.61559874A>G	GRCh37
NC_000017.9:g.58913606A>G	NCBI36
NG_011648.1:g.10441A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.1166A>G MANE Select	ENSP00000290866.4:p.His389Arg
ENST00000290866.9:c.1166A>G	ENSP00000290866.4:p.His389Arg
ENST00000428043.5:c.1166A>G	ENSP00000397593.2:p.His389Arg
ENST00000582678.5:c.*565A>G	ENSP00000462995.1:n.*565A>G
ENST00000584529.5:n.1200A>G
NM_000789.3:c.1166A>G	NP_000780.1:p.His389Arg
XM_005257110.1:c.617A>G	XP_005257167.1:p.His206Arg
NM_000789.4:c.1166A>G MANE Select	NP_000780.1:p.His389Arg
NM_001382700.1:c.599A>G	NP_001369629.1:p.His200Arg
NM_001382701.1:c.314A>G	NP_001369630.1:p.His105Arg