Canonical Allele Identifier: CA400558174

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566328A>T (hg19) ; chr17:g.63488967A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2476A>T MANE Select	ENSP00000290866.4:p.Arg826Trp
ENST00000290863.10:c.754A>T	ENSP00000290863.6:p.Arg252Trp
ENST00000290866.9:c.2476A>T	ENSP00000290866.4:p.Arg826Trp
ENST00000413513.7:c.754A>T	ENSP00000392247.3:p.Arg252Trp
ENST00000428043.5:c.2476A>T	ENSP00000397593.2:p.Arg826Trp
ENST00000577647.2:c.754A>T	ENSP00000464149.1:p.Arg252Trp
ENST00000578839.5:c.*519+176A>T	ENSP00000462110.2:n.*519+176A>T
ENST00000579204.1:c.735A>T	ENSP00000464629.1:n.735A>T
ENST00000579314.5:c.*205A>T	ENSP00000462599.1:n.*205A>T
ENST00000582005.5:c.*396A>T	ENSP00000462002.1:n.*396A>T
ENST00000582761.1:c.244A>T	ENSP00000462909.1:p.Arg82Trp
ENST00000584865.5:n.422A>T
NM_000789.3:c.2476A>T	NP_000780.1:p.Arg826Trp
NM_001178057.1:c.754A>T	NP_001171528.1:p.Arg252Trp
NM_152830.2:c.754A>T	NP_690043.1:p.Arg252Trp
XM_005257110.1:c.1927A>T	XP_005257167.1:p.Arg643Trp
XM_006721737.2:c.814A>T	XP_006721800.2:p.Arg272Trp
XM_006721737.3:c.814A>T	XP_006721800.2:p.Arg272Trp
NM_000789.4:c.2476A>T MANE Select	NP_000780.1:p.Arg826Trp
NM_001178057.2:c.754A>T	NP_001171528.1:p.Arg252Trp
NM_152830.3:c.754A>T	NP_690043.1:p.Arg252Trp
NM_001382700.1:c.1909A>T	NP_001369629.1:p.Arg637Trp
NM_001382701.1:c.1624A>T	NP_001369630.1:p.Arg542Trp
NM_001382702.1:c.379+176A>T	NP_001369631.1:n.379+176A>T
NR_168483.1:n.854A>T