Canonical Allele Identifier: CA400557912

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566068G>C (hg19) ; chr17:g.63488707G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488707G>C , CM000679.2:g.63488707G>C	GRCh38
NC_000017.10:g.61566068G>C , CM000679.1:g.61566068G>C	GRCh37
NC_000017.9:g.58919800G>C	NCBI36
NG_011648.1:g.16635G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2365G>C MANE Select	ENSP00000290866.4:p.Gly789Arg
ENST00000290863.10:c.643G>C	ENSP00000290863.6:p.Gly215Arg
ENST00000290866.9:c.2365G>C	ENSP00000290866.4:p.Gly789Arg
ENST00000413513.7:c.643G>C	ENSP00000392247.3:p.Gly215Arg
ENST00000428043.5:c.2365G>C	ENSP00000397593.2:p.Gly789Arg
ENST00000577647.2:c.643G>C	ENSP00000464149.1:p.Gly215Arg
ENST00000578839.5:c.*435G>C	ENSP00000462110.2:n.*435G>C
ENST00000579204.1:c.624G>C	ENSP00000464629.1:n.624G>C
ENST00000579314.5:c.*94G>C	ENSP00000462599.1:n.*94G>C
ENST00000582005.5:c.*285G>C	ENSP00000462002.1:n.*285G>C
ENST00000582761.1:c.133G>C	ENSP00000462909.1:p.Gly45Arg
ENST00000584865.5:n.311G>C
NM_000789.3:c.2365G>C	NP_000780.1:p.Gly789Arg
NM_001178057.1:c.643G>C	NP_001171528.1:p.Gly215Arg
NM_152830.2:c.643G>C	NP_690043.1:p.Gly215Arg
XM_005257110.1:c.1816G>C	XP_005257167.1:p.Gly606Arg
XM_006721737.2:c.703G>C	XP_006721800.2:p.Gly235Arg
XM_006721737.3:c.703G>C	XP_006721800.2:p.Gly235Arg
NM_000789.4:c.2365G>C MANE Select	NP_000780.1:p.Gly789Arg
NM_001178057.2:c.643G>C	NP_001171528.1:p.Gly215Arg
NM_152830.3:c.643G>C	NP_690043.1:p.Gly215Arg
NM_001382700.1:c.1798G>C	NP_001369629.1:p.Gly600Arg
NM_001382701.1:c.1513G>C	NP_001369630.1:p.Gly505Arg
NM_001382702.1:c.295G>C	NP_001369631.1:p.Gly99Arg
NR_168483.1:n.743G>C