Canonical Allele Identifier: CA400558194

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566337T>G (hg19) ; chr17:g.63488976T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488976T>G , CM000679.2:g.63488976T>G	GRCh38
NC_000017.10:g.61566337T>G , CM000679.1:g.61566337T>G	GRCh37
NC_000017.9:g.58920069T>G	NCBI36
NG_011648.1:g.16904T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2485T>G MANE Select	ENSP00000290866.4:p.Tyr829Asp
ENST00000290863.10:c.763T>G	ENSP00000290863.6:p.Tyr255Asp
ENST00000290866.9:c.2485T>G	ENSP00000290866.4:p.Tyr829Asp
ENST00000413513.7:c.763T>G	ENSP00000392247.3:p.Tyr255Asp
ENST00000428043.5:c.2485T>G	ENSP00000397593.2:p.Tyr829Asp
ENST00000577647.2:c.763T>G	ENSP00000464149.1:p.Tyr255Asp
ENST00000578839.5:c.*519+185T>G	ENSP00000462110.2:n.*519+185T>G
ENST00000579204.1:c.744T>G	ENSP00000464629.1:n.744T>G
ENST00000579314.5:c.*214T>G	ENSP00000462599.1:n.*214T>G
ENST00000582005.5:c.*405T>G	ENSP00000462002.1:n.*405T>G
ENST00000582761.1:c.253T>G	ENSP00000462909.1:p.Tyr85Asp
ENST00000584865.5:n.431T>G
NM_000789.3:c.2485T>G	NP_000780.1:p.Tyr829Asp
NM_001178057.1:c.763T>G	NP_001171528.1:p.Tyr255Asp
NM_152830.2:c.763T>G	NP_690043.1:p.Tyr255Asp
XM_005257110.1:c.1936T>G	XP_005257167.1:p.Tyr646Asp
XM_006721737.2:c.823T>G	XP_006721800.2:p.Tyr275Asp
XM_006721737.3:c.823T>G	XP_006721800.2:p.Tyr275Asp
NM_000789.4:c.2485T>G MANE Select	NP_000780.1:p.Tyr829Asp
NM_001178057.2:c.763T>G	NP_001171528.1:p.Tyr255Asp
NM_152830.3:c.763T>G	NP_690043.1:p.Tyr255Asp
NM_001382700.1:c.1918T>G	NP_001369629.1:p.Tyr640Asp
NM_001382701.1:c.1633T>G	NP_001369630.1:p.Tyr545Asp
NM_001382702.1:c.379+185T>G	NP_001369631.1:n.379+185T>G
NR_168483.1:n.863T>G