Canonical Allele Identifier: CA400557848

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566041T>A (hg19) ; chr17:g.63488680T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488680T>A , CM000679.2:g.63488680T>A	GRCh38
NC_000017.10:g.61566041T>A , CM000679.1:g.61566041T>A	GRCh37
NC_000017.9:g.58919773T>A	NCBI36
NG_011648.1:g.16608T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.2338T>A MANE Select	ENSP00000290866.4:p.Tyr780Asn
ENST00000290863.10:c.616T>A	ENSP00000290863.6:p.Tyr206Asn
ENST00000290866.9:c.2338T>A	ENSP00000290866.4:p.Tyr780Asn
ENST00000413513.7:c.616T>A	ENSP00000392247.3:p.Tyr206Asn
ENST00000428043.5:c.2338T>A	ENSP00000397593.2:p.Tyr780Asn
ENST00000577647.2:c.616T>A	ENSP00000464149.1:p.Tyr206Asn
ENST00000578839.5:c.*408T>A	ENSP00000462110.2:n.*408T>A
ENST00000579204.1:c.597T>A	ENSP00000464629.1:n.597T>A
ENST00000579314.5:c.*67T>A	ENSP00000462599.1:n.*67T>A
ENST00000582005.5:c.*258T>A	ENSP00000462002.1:n.*258T>A
ENST00000582761.1:c.106T>A	ENSP00000462909.1:p.Tyr36Asn
ENST00000584865.5:n.284T>A
NM_000789.3:c.2338T>A	NP_000780.1:p.Tyr780Asn
NM_001178057.1:c.616T>A	NP_001171528.1:p.Tyr206Asn
NM_152830.2:c.616T>A	NP_690043.1:p.Tyr206Asn
XM_005257110.1:c.1789T>A	XP_005257167.1:p.Tyr597Asn
XM_006721737.2:c.676T>A	XP_006721800.2:p.Tyr226Asn
XM_006721737.3:c.676T>A	XP_006721800.2:p.Tyr226Asn
NM_000789.4:c.2338T>A MANE Select	NP_000780.1:p.Tyr780Asn
NM_001178057.2:c.616T>A	NP_001171528.1:p.Tyr206Asn
NM_152830.3:c.616T>A	NP_690043.1:p.Tyr206Asn
NM_001382700.1:c.1771T>A	NP_001369629.1:p.Tyr591Asn
NM_001382701.1:c.1486T>A	NP_001369630.1:p.Tyr496Asn
NM_001382702.1:c.268T>A	NP_001369631.1:p.Tyr90Asn
NR_168483.1:n.716T>A