Canonical Allele Identifier: CA400556884

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61564413A>C (hg19) ; chr17:g.63487052A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63487052A>C , CM000679.2:g.63487052A>C	GRCh38
NC_000017.10:g.61564413A>C , CM000679.1:g.61564413A>C	GRCh37
NC_000017.9:g.58918145A>C	NCBI36
NG_011648.1:g.14980A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2284A>C MANE Select	ENSP00000290866.4:p.Ser762Arg
ENST00000290863.10:c.562A>C	ENSP00000290863.6:p.Ser188Arg
ENST00000290866.9:c.2284A>C	ENSP00000290866.4:p.Ser762Arg
ENST00000413513.7:c.562A>C	ENSP00000392247.3:p.Ser188Arg
ENST00000428043.5:c.2284A>C	ENSP00000397593.2:p.Ser762Arg
ENST00000577647.2:c.562A>C	ENSP00000464149.1:p.Ser188Arg
ENST00000578839.5:c.*354A>C	ENSP00000462110.2:n.*354A>C
ENST00000579204.1:c.465A>C	ENSP00000464629.1:n.465A>C
ENST00000579314.5:c.562A>C	ENSP00000462599.1:p.Ser188Arg
ENST00000579726.5:c.846A>C
ENST00000582005.5:c.*204A>C	ENSP00000462002.1:n.*204A>C
ENST00000582761.1:c.52A>C	ENSP00000462909.1:p.Ser18Arg
ENST00000584865.5:n.230A>C
NM_000789.3:c.2284A>C	NP_000780.1:p.Ser762Arg
NM_001178057.1:c.562A>C	NP_001171528.1:p.Ser188Arg
NM_152830.2:c.562A>C	NP_690043.1:p.Ser188Arg
XM_005257110.1:c.1735A>C	XP_005257167.1:p.Ser579Arg
XM_006721737.2:c.622A>C	XP_006721800.2:p.Ser208Arg
XM_006721737.3:c.622A>C	XP_006721800.2:p.Ser208Arg
NM_000789.4:c.2284A>C MANE Select	NP_000780.1:p.Ser762Arg
NM_001178057.2:c.562A>C	NP_001171528.1:p.Ser188Arg
NM_152830.3:c.562A>C	NP_690043.1:p.Ser188Arg
NM_001382700.1:c.1717A>C	NP_001369629.1:p.Ser573Arg
NM_001382701.1:c.1432A>C	NP_001369630.1:p.Ser478Arg
NM_001382702.1:c.214A>C	NP_001369631.1:p.Ser72Arg
NR_168483.1:n.584A>C