Canonical Allele Identifier: CA501187957

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566328A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488967A>C , CM000679.2:g.63488967A>C	GRCh38
NC_000017.10:g.61566328A>C , CM000679.1:g.61566328A>C	GRCh37
NC_000017.9:g.58920060A>C	NCBI36
NG_011648.1:g.16895A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2476A>C MANE Select	ENSP00000290866.4:p.Arg826=
ENST00000290863.10:c.754A>C	ENSP00000290863.6:p.Arg252=
ENST00000290866.9:c.2476A>C	ENSP00000290866.4:p.Arg826=
ENST00000413513.7:c.754A>C	ENSP00000392247.3:p.Arg252=
ENST00000428043.5:c.2476A>C	ENSP00000397593.2:p.Arg826=
ENST00000577647.2:c.754A>C	ENSP00000464149.1:p.Arg252=
ENST00000578839.5:c.*519+176A>C	ENSP00000462110.2:n.*519+176A>C
ENST00000579204.1:c.735A>C	ENSP00000464629.1:n.735A>C
ENST00000579314.5:c.*205A>C	ENSP00000462599.1:n.*205A>C
ENST00000582005.5:c.*396A>C	ENSP00000462002.1:n.*396A>C
ENST00000582761.1:c.244A>C	ENSP00000462909.1:p.Arg82=
ENST00000584865.5:n.422A>C
NM_000789.3:c.2476A>C	NP_000780.1:p.Arg826=
NM_001178057.1:c.754A>C	NP_001171528.1:p.Arg252=
NM_152830.2:c.754A>C	NP_690043.1:p.Arg252=
XM_005257110.1:c.1927A>C	XP_005257167.1:p.Arg643=
XM_006721737.2:c.814A>C	XP_006721800.2:p.Arg272=
XM_006721737.3:c.814A>C	XP_006721800.2:p.Arg272=
NM_000789.4:c.2476A>C MANE Select	NP_000780.1:p.Arg826=
NM_001178057.2:c.754A>C	NP_001171528.1:p.Arg252=
NM_152830.3:c.754A>C	NP_690043.1:p.Arg252=
NM_001382700.1:c.1909A>C	NP_001369629.1:p.Arg637=
NM_001382701.1:c.1624A>C	NP_001369630.1:p.Arg542=
NM_001382702.1:c.379+176A>C	NP_001369631.1:n.379+176A>C
NR_168483.1:n.854A>C