Canonical Allele Identifier: CA400556232

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61564035G>T (hg19) ; chr17:g.63486674G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486674G>T , CM000679.2:g.63486674G>T	GRCh38
NC_000017.10:g.61564035G>T , CM000679.1:g.61564035G>T	GRCh37
NC_000017.9:g.58917767G>T	NCBI36
NG_011648.1:g.14602G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2176G>T MANE Select	ENSP00000290866.4:p.Asp726Tyr
ENST00000290863.10:c.454G>T	ENSP00000290863.6:p.Asp152Tyr
ENST00000290866.9:c.2176G>T	ENSP00000290866.4:p.Asp726Tyr
ENST00000413513.7:c.454G>T	ENSP00000392247.3:p.Asp152Tyr
ENST00000428043.5:c.2176G>T	ENSP00000397593.2:p.Asp726Tyr
ENST00000577647.2:c.454G>T	ENSP00000464149.1:p.Asp152Tyr
ENST00000578839.5:c.*246G>T	ENSP00000462110.2:n.*246G>T
ENST00000579204.1:c.357G>T	ENSP00000464629.1:n.357G>T
ENST00000579314.5:c.454G>T	ENSP00000462599.1:p.Asp152Tyr
ENST00000579726.5:c.738G>T
ENST00000582005.5:c.*96G>T	ENSP00000462002.1:n.*96G>T
NM_000789.3:c.2176G>T	NP_000780.1:p.Asp726Tyr
NM_001178057.1:c.454G>T	NP_001171528.1:p.Asp152Tyr
NM_152830.2:c.454G>T	NP_690043.1:p.Asp152Tyr
XM_005257110.1:c.1627G>T	XP_005257167.1:p.Asp543Tyr
XM_006721737.2:c.514G>T	XP_006721800.2:p.Asp172Tyr
XM_006721737.3:c.514G>T	XP_006721800.2:p.Asp172Tyr
NM_000789.4:c.2176G>T MANE Select	NP_000780.1:p.Asp726Tyr
NM_001178057.2:c.454G>T	NP_001171528.1:p.Asp152Tyr
NM_152830.3:c.454G>T	NP_690043.1:p.Asp152Tyr
NM_001382700.1:c.1609G>T	NP_001369629.1:p.Asp537Tyr
NM_001382701.1:c.1324G>T	NP_001369630.1:p.Asp442Tyr
NM_001382702.1:c.106G>T	NP_001369631.1:p.Asp36Tyr
NR_168483.1:n.476G>T