Canonical Allele Identifier: CA400558165

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566325T>C (hg19) ; chr17:g.63488964T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488964T>C , CM000679.2:g.63488964T>C	GRCh38
NC_000017.10:g.61566325T>C , CM000679.1:g.61566325T>C	GRCh37
NC_000017.9:g.58920057T>C	NCBI36
NG_011648.1:g.16892T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2473T>C MANE Select	ENSP00000290866.4:p.Trp825Arg
ENST00000290863.10:c.751T>C	ENSP00000290863.6:p.Trp251Arg
ENST00000290866.9:c.2473T>C	ENSP00000290866.4:p.Trp825Arg
ENST00000413513.7:c.751T>C	ENSP00000392247.3:p.Trp251Arg
ENST00000428043.5:c.2473T>C	ENSP00000397593.2:p.Trp825Arg
ENST00000577647.2:c.751T>C	ENSP00000464149.1:p.Trp251Arg
ENST00000578839.5:c.*519+173T>C	ENSP00000462110.2:n.*519+173T>C
ENST00000579204.1:c.732T>C	ENSP00000464629.1:n.732T>C
ENST00000579314.5:c.*202T>C	ENSP00000462599.1:n.*202T>C
ENST00000582005.5:c.*393T>C	ENSP00000462002.1:n.*393T>C
ENST00000582761.1:c.241T>C	ENSP00000462909.1:p.Trp81Arg
ENST00000584865.5:n.419T>C
NM_000789.3:c.2473T>C	NP_000780.1:p.Trp825Arg
NM_001178057.1:c.751T>C	NP_001171528.1:p.Trp251Arg
NM_152830.2:c.751T>C	NP_690043.1:p.Trp251Arg
XM_005257110.1:c.1924T>C	XP_005257167.1:p.Trp642Arg
XM_006721737.2:c.811T>C	XP_006721800.2:p.Trp271Arg
XM_006721737.3:c.811T>C	XP_006721800.2:p.Trp271Arg
NM_000789.4:c.2473T>C MANE Select	NP_000780.1:p.Trp825Arg
NM_001178057.2:c.751T>C	NP_001171528.1:p.Trp251Arg
NM_152830.3:c.751T>C	NP_690043.1:p.Trp251Arg
NM_001382700.1:c.1906T>C	NP_001369629.1:p.Trp636Arg
NM_001382701.1:c.1621T>C	NP_001369630.1:p.Trp541Arg
NM_001382702.1:c.379+173T>C	NP_001369631.1:n.379+173T>C
NR_168483.1:n.851T>C