Canonical Allele Identifier: CA400558035

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566125C>G (hg19) ; chr17:g.63488764C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488764C>G , CM000679.2:g.63488764C>G	GRCh38
NC_000017.10:g.61566125C>G , CM000679.1:g.61566125C>G	GRCh37
NC_000017.9:g.58919857C>G	NCBI36
NG_011648.1:g.16692C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2422C>G MANE Select	ENSP00000290866.4:p.Leu808Val
ENST00000290863.10:c.700C>G	ENSP00000290863.6:p.Leu234Val
ENST00000290866.9:c.2422C>G	ENSP00000290866.4:p.Leu808Val
ENST00000413513.7:c.700C>G	ENSP00000392247.3:p.Leu234Val
ENST00000428043.5:c.2422C>G	ENSP00000397593.2:p.Leu808Val
ENST00000577647.2:c.700C>G	ENSP00000464149.1:p.Leu234Val
ENST00000578839.5:c.*492C>G	ENSP00000462110.2:n.*492C>G
ENST00000579204.1:c.681C>G	ENSP00000464629.1:n.681C>G
ENST00000579314.5:c.*151C>G	ENSP00000462599.1:n.*151C>G
ENST00000582005.5:c.*342C>G	ENSP00000462002.1:n.*342C>G
ENST00000582761.1:c.190C>G	ENSP00000462909.1:p.Leu64Val
ENST00000584865.5:n.368C>G
NM_000789.3:c.2422C>G	NP_000780.1:p.Leu808Val
NM_001178057.1:c.700C>G	NP_001171528.1:p.Leu234Val
NM_152830.2:c.700C>G	NP_690043.1:p.Leu234Val
XM_005257110.1:c.1873C>G	XP_005257167.1:p.Leu625Val
XM_006721737.2:c.760C>G	XP_006721800.2:p.Leu254Val
XM_006721737.3:c.760C>G	XP_006721800.2:p.Leu254Val
NM_000789.4:c.2422C>G MANE Select	NP_000780.1:p.Leu808Val
NM_001178057.2:c.700C>G	NP_001171528.1:p.Leu234Val
NM_152830.3:c.700C>G	NP_690043.1:p.Leu234Val
NM_001382700.1:c.1855C>G	NP_001369629.1:p.Leu619Val
NM_001382701.1:c.1570C>G	NP_001369630.1:p.Leu524Val
NM_001382702.1:c.352C>G	NP_001369631.1:p.Leu118Val
NR_168483.1:n.800C>G