Canonical Allele Identifier: CA400557933

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566078A>G (hg19) ; chr17:g.63488717A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488717A>G , CM000679.2:g.63488717A>G	GRCh38
NC_000017.10:g.61566078A>G , CM000679.1:g.61566078A>G	GRCh37
NC_000017.9:g.58919810A>G	NCBI36
NG_011648.1:g.16645A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2375A>G MANE Select	ENSP00000290866.4:p.Asp792Gly
ENST00000290863.10:c.653A>G	ENSP00000290863.6:p.Asp218Gly
ENST00000290866.9:c.2375A>G	ENSP00000290866.4:p.Asp792Gly
ENST00000413513.7:c.653A>G	ENSP00000392247.3:p.Asp218Gly
ENST00000428043.5:c.2375A>G	ENSP00000397593.2:p.Asp792Gly
ENST00000577647.2:c.653A>G	ENSP00000464149.1:p.Asp218Gly
ENST00000578839.5:c.*445A>G	ENSP00000462110.2:n.*445A>G
ENST00000579204.1:c.634A>G	ENSP00000464629.1:n.634A>G
ENST00000579314.5:c.*104A>G	ENSP00000462599.1:n.*104A>G
ENST00000582005.5:c.*295A>G	ENSP00000462002.1:n.*295A>G
ENST00000582761.1:c.143A>G	ENSP00000462909.1:p.Asp48Gly
ENST00000584865.5:n.321A>G
NM_000789.3:c.2375A>G	NP_000780.1:p.Asp792Gly
NM_001178057.1:c.653A>G	NP_001171528.1:p.Asp218Gly
NM_152830.2:c.653A>G	NP_690043.1:p.Asp218Gly
XM_005257110.1:c.1826A>G	XP_005257167.1:p.Asp609Gly
XM_006721737.2:c.713A>G	XP_006721800.2:p.Asp238Gly
XM_006721737.3:c.713A>G	XP_006721800.2:p.Asp238Gly
NM_000789.4:c.2375A>G MANE Select	NP_000780.1:p.Asp792Gly
NM_001178057.2:c.653A>G	NP_001171528.1:p.Asp218Gly
NM_152830.3:c.653A>G	NP_690043.1:p.Asp218Gly
NM_001382700.1:c.1808A>G	NP_001369629.1:p.Asp603Gly
NM_001382701.1:c.1523A>G	NP_001369630.1:p.Asp508Gly
NM_001382702.1:c.305A>G	NP_001369631.1:p.Asp102Gly
NR_168483.1:n.753A>G