Canonical Allele Identifier: CA501187409

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566124A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488763A>G , CM000679.2:g.63488763A>G	GRCh38
NC_000017.10:g.61566124A>G , CM000679.1:g.61566124A>G	GRCh37
NC_000017.9:g.58919856A>G	NCBI36
NG_011648.1:g.16691A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2421A>G MANE Select	ENSP00000290866.4:p.Glu807=
ENST00000290863.10:c.699A>G	ENSP00000290863.6:p.Glu233=
ENST00000290866.9:c.2421A>G	ENSP00000290866.4:p.Glu807=
ENST00000413513.7:c.699A>G	ENSP00000392247.3:p.Glu233=
ENST00000428043.5:c.2421A>G	ENSP00000397593.2:p.Glu807=
ENST00000577647.2:c.699A>G	ENSP00000464149.1:p.Glu233=
ENST00000578839.5:c.*491A>G	ENSP00000462110.2:n.*491A>G
ENST00000579204.1:c.680A>G	ENSP00000464629.1:n.680A>G
ENST00000579314.5:c.*150A>G	ENSP00000462599.1:n.*150A>G
ENST00000582005.5:c.*341A>G	ENSP00000462002.1:n.*341A>G
ENST00000582761.1:c.189A>G	ENSP00000462909.1:p.Glu63=
ENST00000584865.5:n.367A>G
NM_000789.3:c.2421A>G	NP_000780.1:p.Glu807=
NM_001178057.1:c.699A>G	NP_001171528.1:p.Glu233=
NM_152830.2:c.699A>G	NP_690043.1:p.Glu233=
XM_005257110.1:c.1872A>G	XP_005257167.1:p.Glu624=
XM_006721737.2:c.759A>G	XP_006721800.2:p.Glu253=
XM_006721737.3:c.759A>G	XP_006721800.2:p.Glu253=
NM_000789.4:c.2421A>G MANE Select	NP_000780.1:p.Glu807=
NM_001178057.2:c.699A>G	NP_001171528.1:p.Glu233=
NM_152830.3:c.699A>G	NP_690043.1:p.Glu233=
NM_001382700.1:c.1854A>G	NP_001369629.1:p.Glu618=
NM_001382701.1:c.1569A>G	NP_001369630.1:p.Glu523=
NM_001382702.1:c.351A>G	NP_001369631.1:p.Glu117=
NR_168483.1:n.799A>G