Canonical Allele Identifier: CA501186795

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566037G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488676G>C , CM000679.2:g.63488676G>C	GRCh38
NC_000017.10:g.61566037G>C , CM000679.1:g.61566037G>C	GRCh37
NC_000017.9:g.58919769G>C	NCBI36
NG_011648.1:g.16604G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.2334G>C MANE Select	ENSP00000290866.4:p.Arg778=
ENST00000290863.10:c.612G>C	ENSP00000290863.6:p.Arg204=
ENST00000290866.9:c.2334G>C	ENSP00000290866.4:p.Arg778=
ENST00000413513.7:c.612G>C	ENSP00000392247.3:p.Arg204=
ENST00000428043.5:c.2334G>C	ENSP00000397593.2:p.Arg778=
ENST00000577647.2:c.612G>C	ENSP00000464149.1:p.Arg204=
ENST00000578839.5:c.*404G>C	ENSP00000462110.2:n.*404G>C
ENST00000579204.1:c.593G>C	ENSP00000464629.1:n.593G>C
ENST00000579314.5:c.*63G>C	ENSP00000462599.1:n.*63G>C
ENST00000582005.5:c.*254G>C	ENSP00000462002.1:n.*254G>C
ENST00000582761.1:c.102G>C	ENSP00000462909.1:p.Arg34=
ENST00000584865.5:n.280G>C
NM_000789.3:c.2334G>C	NP_000780.1:p.Arg778=
NM_001178057.1:c.612G>C	NP_001171528.1:p.Arg204=
NM_152830.2:c.612G>C	NP_690043.1:p.Arg204=
XM_005257110.1:c.1785G>C	XP_005257167.1:p.Arg595=
XM_006721737.2:c.672G>C	XP_006721800.2:p.Arg224=
XM_006721737.3:c.672G>C	XP_006721800.2:p.Arg224=
NM_000789.4:c.2334G>C MANE Select	NP_000780.1:p.Arg778=
NM_001178057.2:c.612G>C	NP_001171528.1:p.Arg204=
NM_152830.3:c.612G>C	NP_690043.1:p.Arg204=
NM_001382700.1:c.1767G>C	NP_001369629.1:p.Arg589=
NM_001382701.1:c.1482G>C	NP_001369630.1:p.Arg494=
NM_001382702.1:c.264G>C	NP_001369631.1:p.Arg88=
NR_168483.1:n.712G>C