Canonical Allele Identifier: CA400566619

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574178T>G (hg19) ; chr17:g.63496817T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496817T>G , CM000679.2:g.63496817T>G	GRCh38
NC_000017.10:g.61574178T>G , CM000679.1:g.61574178T>G	GRCh37
NC_000017.9:g.58927910T>G	NCBI36
NG_011648.1:g.24745T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3523T>G MANE Select	ENSP00000290866.4:p.Phe1175Val
ENST00000290863.10:c.1801T>G	ENSP00000290863.6:p.Phe601Val
ENST00000290866.9:c.3523T>G	ENSP00000290866.4:p.Phe1175Val
ENST00000413513.7:c.1678T>G	ENSP00000392247.3:p.Phe560Val
ENST00000428043.5:c.3523T>G	ENSP00000397593.2:p.Phe1175Val
ENST00000577418.5:n.533T>G
ENST00000577647.2:c.1801T>G	ENSP00000464149.1:p.Phe601Val
ENST00000578839.5:c.*1278T>G	ENSP00000462110.2:n.*1278T>G
ENST00000579314.5:c.*1252T>G	ENSP00000462599.1:n.*1252T>G
ENST00000579409.1:c.210T>G
ENST00000582244.1:n.397T>G
NM_000789.3:c.3523T>G	NP_000780.1:p.Phe1175Val
NM_001178057.1:c.1678T>G	NP_001171528.1:p.Phe560Val
NM_152830.2:c.1801T>G	NP_690043.1:p.Phe601Val
XM_005257110.1:c.2974T>G	XP_005257167.1:p.Phe992Val
XM_006721737.2:c.1861T>G	XP_006721800.2:p.Phe621Val
XM_006721737.3:c.1861T>G	XP_006721800.2:p.Phe621Val
NM_000789.4:c.3523T>G MANE Select	NP_000780.1:p.Phe1175Val
NM_001178057.2:c.1678T>G	NP_001171528.1:p.Phe560Val
NM_152830.3:c.1801T>G	NP_690043.1:p.Phe601Val
NM_001382700.1:c.2956T>G	NP_001369629.1:p.Phe986Val
NM_001382701.1:c.2671T>G	NP_001369630.1:p.Phe891Val
NM_001382702.1:c.1138T>G	NP_001369631.1:p.Phe380Val
NR_168483.1:n.1901T>G