Canonical Allele Identifier: CA8699946

Gene: ACE

Linked Data

• dbSNP Id: rs745422986
• ExAC: 17:61564005 A / G
• gnomAD v2: 17-61564005-A-G
• gnomAD v3: 17-63486644-A-G
• gnomAD v4: 17-63486644-A-G
• MyVariant Identifiers: chr17:g.61564005A>G (hg19) ; chr17:g.63486644A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486644A>G , CM000679.2:g.63486644A>G	GRCh38
NC_000017.10:g.61564005A>G , CM000679.1:g.61564005A>G	GRCh37
NC_000017.9:g.58917737A>G	NCBI36
NG_011648.1:g.14572A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2146A>G MANE Select	ENSP00000290866.4:p.Thr716Ala
ENST00000290863.10:c.424A>G	ENSP00000290863.6:p.Thr142Ala
ENST00000290866.9:c.2146A>G	ENSP00000290866.4:p.Thr716Ala
ENST00000413513.7:c.424A>G	ENSP00000392247.3:p.Thr142Ala
ENST00000428043.5:c.2146A>G	ENSP00000397593.2:p.Thr716Ala
ENST00000577647.2:c.424A>G	ENSP00000464149.1:p.Thr142Ala
ENST00000578839.5:c.*216A>G	ENSP00000462110.2:n.*216A>G
ENST00000579204.1:c.327A>G	ENSP00000464629.1:n.327A>G
ENST00000579314.5:c.424A>G	ENSP00000462599.1:p.Thr142Ala
ENST00000579726.5:c.708A>G
ENST00000582005.5:c.*66A>G	ENSP00000462002.1:n.*66A>G
NM_000789.3:c.2146A>G	NP_000780.1:p.Thr716Ala
NM_001178057.1:c.424A>G	NP_001171528.1:p.Thr142Ala
NM_152830.2:c.424A>G	NP_690043.1:p.Thr142Ala
XM_005257110.1:c.1597A>G	XP_005257167.1:p.Thr533Ala
XM_006721737.2:c.484A>G	XP_006721800.2:p.Thr162Ala
XM_006721737.3:c.484A>G	XP_006721800.2:p.Thr162Ala
NM_000789.4:c.2146A>G MANE Select	NP_000780.1:p.Thr716Ala
NM_001178057.2:c.424A>G	NP_001171528.1:p.Thr142Ala
NM_152830.3:c.424A>G	NP_690043.1:p.Thr142Ala
NM_001382700.1:c.1579A>G	NP_001369629.1:p.Thr527Ala
NM_001382701.1:c.1294A>G	NP_001369630.1:p.Thr432Ala
NM_001382702.1:c.76A>G	NP_001369631.1:p.Thr26Ala
NR_168483.1:n.446A>G