Canonical Allele Identifier: CA400567694

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574314G>T (hg19) ; chr17:g.63496953G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496953G>T , CM000679.2:g.63496953G>T	GRCh38
NC_000017.10:g.61574314G>T , CM000679.1:g.61574314G>T	GRCh37
NC_000017.9:g.58928046G>T	NCBI36
NG_011648.1:g.24881G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3659G>T MANE Select	ENSP00000290866.4:p.Gly1220Val
ENST00000290863.10:c.1937G>T	ENSP00000290863.6:p.Gly646Val
ENST00000290866.9:c.3659G>T	ENSP00000290866.4:p.Gly1220Val
ENST00000413513.7:c.1814G>T	ENSP00000392247.3:p.Gly605Val
ENST00000428043.5:c.3659G>T	ENSP00000397593.2:p.Gly1220Val
ENST00000577418.5:n.669G>T
ENST00000577647.2:c.1937G>T	ENSP00000464149.1:p.Gly646Val
ENST00000578839.5:c.*1414G>T	ENSP00000462110.2:n.*1414G>T
ENST00000579314.5:c.*1388G>T	ENSP00000462599.1:n.*1388G>T
ENST00000579409.1:c.346G>T
ENST00000582244.1:n.533G>T
NM_000789.3:c.3659G>T	NP_000780.1:p.Gly1220Val
NM_001178057.1:c.1814G>T	NP_001171528.1:p.Gly605Val
NM_152830.2:c.1937G>T	NP_690043.1:p.Gly646Val
XM_005257110.1:c.3110G>T	XP_005257167.1:p.Gly1037Val
XM_006721737.2:c.1997G>T	XP_006721800.2:p.Gly666Val
XM_006721737.3:c.1997G>T	XP_006721800.2:p.Gly666Val
NM_000789.4:c.3659G>T MANE Select	NP_000780.1:p.Gly1220Val
NM_001178057.2:c.1814G>T	NP_001171528.1:p.Gly605Val
NM_152830.3:c.1937G>T	NP_690043.1:p.Gly646Val
NM_001382700.1:c.3092G>T	NP_001369629.1:p.Gly1031Val
NM_001382701.1:c.2807G>T	NP_001369630.1:p.Gly936Val
NM_001382702.1:c.1274G>T	NP_001369631.1:p.Gly425Val
NR_168483.1:n.2037G>T