Canonical Allele Identifier: CA400557855

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566043T>G (hg19) ; chr17:g.63488682T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488682T>G , CM000679.2:g.63488682T>G	GRCh38
NC_000017.10:g.61566043T>G , CM000679.1:g.61566043T>G	GRCh37
NC_000017.9:g.58919775T>G	NCBI36
NG_011648.1:g.16610T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.2340T>G MANE Select	ENSP00000290866.4:p.Tyr780Ter
ENST00000290863.10:c.618T>G	ENSP00000290863.6:p.Tyr206Ter
ENST00000290866.9:c.2340T>G	ENSP00000290866.4:p.Tyr780Ter
ENST00000413513.7:c.618T>G	ENSP00000392247.3:p.Tyr206Ter
ENST00000428043.5:c.2340T>G	ENSP00000397593.2:p.Tyr780Ter
ENST00000577647.2:c.618T>G	ENSP00000464149.1:p.Tyr206Ter
ENST00000578839.5:c.*410T>G	ENSP00000462110.2:n.*410T>G
ENST00000579204.1:c.599T>G	ENSP00000464629.1:n.599T>G
ENST00000579314.5:c.*69T>G	ENSP00000462599.1:n.*69T>G
ENST00000582005.5:c.*260T>G	ENSP00000462002.1:n.*260T>G
ENST00000582761.1:c.108T>G	ENSP00000462909.1:p.Tyr36Ter
ENST00000584865.5:n.286T>G
NM_000789.3:c.2340T>G	NP_000780.1:p.Tyr780Ter
NM_001178057.1:c.618T>G	NP_001171528.1:p.Tyr206Ter
NM_152830.2:c.618T>G	NP_690043.1:p.Tyr206Ter
XM_005257110.1:c.1791T>G	XP_005257167.1:p.Tyr597Ter
XM_006721737.2:c.678T>G	XP_006721800.2:p.Tyr226Ter
XM_006721737.3:c.678T>G	XP_006721800.2:p.Tyr226Ter
NM_000789.4:c.2340T>G MANE Select	NP_000780.1:p.Tyr780Ter
NM_001178057.2:c.618T>G	NP_001171528.1:p.Tyr206Ter
NM_152830.3:c.618T>G	NP_690043.1:p.Tyr206Ter
NM_001382700.1:c.1773T>G	NP_001369629.1:p.Tyr591Ter
NM_001382701.1:c.1488T>G	NP_001369630.1:p.Tyr496Ter
NM_001382702.1:c.270T>G	NP_001369631.1:p.Tyr90Ter
NR_168483.1:n.718T>G