Canonical Allele Identifier: CA400558027

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566122G>C (hg19) ; chr17:g.63488761G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488761G>C , CM000679.2:g.63488761G>C	GRCh38
NC_000017.10:g.61566122G>C , CM000679.1:g.61566122G>C	GRCh37
NC_000017.9:g.58919854G>C	NCBI36
NG_011648.1:g.16689G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2419G>C MANE Select	ENSP00000290866.4:p.Glu807Gln
ENST00000290863.10:c.697G>C	ENSP00000290863.6:p.Glu233Gln
ENST00000290866.9:c.2419G>C	ENSP00000290866.4:p.Glu807Gln
ENST00000413513.7:c.697G>C	ENSP00000392247.3:p.Glu233Gln
ENST00000428043.5:c.2419G>C	ENSP00000397593.2:p.Glu807Gln
ENST00000577647.2:c.697G>C	ENSP00000464149.1:p.Glu233Gln
ENST00000578839.5:c.*489G>C	ENSP00000462110.2:n.*489G>C
ENST00000579204.1:c.678G>C	ENSP00000464629.1:n.678G>C
ENST00000579314.5:c.*148G>C	ENSP00000462599.1:n.*148G>C
ENST00000582005.5:c.*339G>C	ENSP00000462002.1:n.*339G>C
ENST00000582761.1:c.187G>C	ENSP00000462909.1:p.Glu63Gln
ENST00000584865.5:n.365G>C
NM_000789.3:c.2419G>C	NP_000780.1:p.Glu807Gln
NM_001178057.1:c.697G>C	NP_001171528.1:p.Glu233Gln
NM_152830.2:c.697G>C	NP_690043.1:p.Glu233Gln
XM_005257110.1:c.1870G>C	XP_005257167.1:p.Glu624Gln
XM_006721737.2:c.757G>C	XP_006721800.2:p.Glu253Gln
XM_006721737.3:c.757G>C	XP_006721800.2:p.Glu253Gln
NM_000789.4:c.2419G>C MANE Select	NP_000780.1:p.Glu807Gln
NM_001178057.2:c.697G>C	NP_001171528.1:p.Glu233Gln
NM_152830.3:c.697G>C	NP_690043.1:p.Glu233Gln
NM_001382700.1:c.1852G>C	NP_001369629.1:p.Glu618Gln
NM_001382701.1:c.1567G>C	NP_001369630.1:p.Glu523Gln
NM_001382702.1:c.349G>C	NP_001369631.1:p.Glu117Gln
NR_168483.1:n.797G>C