Canonical Allele Identifier: CA400567263

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574254A>G (hg19) ; chr17:g.63496893A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496893A>G , CM000679.2:g.63496893A>G	GRCh38
NC_000017.10:g.61574254A>G , CM000679.1:g.61574254A>G	GRCh37
NC_000017.9:g.58927986A>G	NCBI36
NG_011648.1:g.24821A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3599A>G MANE Select	ENSP00000290866.4:p.Tyr1200Cys
ENST00000290863.10:c.1877A>G	ENSP00000290863.6:p.Tyr626Cys
ENST00000290866.9:c.3599A>G	ENSP00000290866.4:p.Tyr1200Cys
ENST00000413513.7:c.1754A>G	ENSP00000392247.3:p.Tyr585Cys
ENST00000428043.5:c.3599A>G	ENSP00000397593.2:p.Tyr1200Cys
ENST00000577418.5:n.609A>G
ENST00000577647.2:c.1877A>G	ENSP00000464149.1:p.Tyr626Cys
ENST00000578839.5:c.*1354A>G	ENSP00000462110.2:n.*1354A>G
ENST00000579314.5:c.*1328A>G	ENSP00000462599.1:n.*1328A>G
ENST00000579409.1:c.286A>G
ENST00000582244.1:n.473A>G
NM_000789.3:c.3599A>G	NP_000780.1:p.Tyr1200Cys
NM_001178057.1:c.1754A>G	NP_001171528.1:p.Tyr585Cys
NM_152830.2:c.1877A>G	NP_690043.1:p.Tyr626Cys
XM_005257110.1:c.3050A>G	XP_005257167.1:p.Tyr1017Cys
XM_006721737.2:c.1937A>G	XP_006721800.2:p.Tyr646Cys
XM_006721737.3:c.1937A>G	XP_006721800.2:p.Tyr646Cys
NM_000789.4:c.3599A>G MANE Select	NP_000780.1:p.Tyr1200Cys
NM_001178057.2:c.1754A>G	NP_001171528.1:p.Tyr585Cys
NM_152830.3:c.1877A>G	NP_690043.1:p.Tyr626Cys
NM_001382700.1:c.3032A>G	NP_001369629.1:p.Tyr1011Cys
NM_001382701.1:c.2747A>G	NP_001369630.1:p.Tyr916Cys
NM_001382702.1:c.1214A>G	NP_001369631.1:p.Tyr405Cys
NR_168483.1:n.1977A>G