Canonical Allele Identifier: CA400558091

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566149A>G (hg19) ; chr17:g.63488788A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488788A>G , CM000679.2:g.63488788A>G	GRCh38
NC_000017.10:g.61566149A>G , CM000679.1:g.61566149A>G	GRCh37
NC_000017.9:g.58919881A>G	NCBI36
NG_011648.1:g.16716A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2446A>G MANE Select	ENSP00000290866.4:p.Asn816Asp
ENST00000290863.10:c.724A>G	ENSP00000290863.6:p.Asn242Asp
ENST00000290866.9:c.2446A>G	ENSP00000290866.4:p.Asn816Asp
ENST00000413513.7:c.724A>G	ENSP00000392247.3:p.Asn242Asp
ENST00000428043.5:c.2446A>G	ENSP00000397593.2:p.Asn816Asp
ENST00000577647.2:c.724A>G	ENSP00000464149.1:p.Asn242Asp
ENST00000578839.5:c.*516A>G	ENSP00000462110.2:n.*516A>G
ENST00000579204.1:c.705A>G	ENSP00000464629.1:n.705A>G
ENST00000579314.5:c.*175A>G	ENSP00000462599.1:n.*175A>G
ENST00000582005.5:c.*366A>G	ENSP00000462002.1:n.*366A>G
ENST00000582761.1:c.214A>G	ENSP00000462909.1:p.Asn72Asp
ENST00000584865.5:n.392A>G
NM_000789.3:c.2446A>G	NP_000780.1:p.Asn816Asp
NM_001178057.1:c.724A>G	NP_001171528.1:p.Asn242Asp
NM_152830.2:c.724A>G	NP_690043.1:p.Asn242Asp
XM_005257110.1:c.1897A>G	XP_005257167.1:p.Asn633Asp
XM_006721737.2:c.784A>G	XP_006721800.2:p.Asn262Asp
XM_006721737.3:c.784A>G	XP_006721800.2:p.Asn262Asp
NM_000789.4:c.2446A>G MANE Select	NP_000780.1:p.Asn816Asp
NM_001178057.2:c.724A>G	NP_001171528.1:p.Asn242Asp
NM_152830.3:c.724A>G	NP_690043.1:p.Asn242Asp
NM_001382700.1:c.1879A>G	NP_001369629.1:p.Asn627Asp
NM_001382701.1:c.1594A>G	NP_001369630.1:p.Asn532Asp
NM_001382702.1:c.376A>G	NP_001369631.1:p.Asn126Asp
NR_168483.1:n.824A>G