Canonical Allele Identifier: CA2269945971

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488734_63488737delinsATCC , CM000679.2:g.63488734_63488737delinsATCC	GRCh38
NC_000017.10:g.61566095_61566098delinsATCC , CM000679.1:g.61566095_61566098delinsATCC	GRCh37
NC_000017.9:g.58919827_58919830delinsATCC	NCBI36
NG_011648.1:g.16662_16665delinsATCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2392_2395delinsATCC MANE Select	ENSP00000290866.4:p.Ile798=
ENST00000290863.10:c.670_673delinsATCC	ENSP00000290863.6:p.Ile224=
ENST00000290866.9:c.2392_2395delinsATCC	ENSP00000290866.4:p.Ile798=
ENST00000413513.7:c.670_673delinsATCC	ENSP00000392247.3:p.Ile224=
ENST00000428043.5:c.2392_2395delinsATCC	ENSP00000397593.2:p.Ile798=
ENST00000577647.2:c.670_673delinsATCC	ENSP00000464149.1:p.Ile224=
ENST00000578839.5:c.*462_*465delinsATCC	ENSP00000462110.2:n.*462_*465delinsATCC
ENST00000579204.1:c.651_654delinsATCC	ENSP00000464629.1:n.651_654delinsATCC
ENST00000579314.5:c.*121_*124delinsATCC	ENSP00000462599.1:n.*121_*124delinsATCC
ENST00000582005.5:c.*312_*315delinsATCC	ENSP00000462002.1:n.*312_*315delinsATCC
ENST00000582761.1:c.160_163delinsATCC	ENSP00000462909.1:p.Ile54=
ENST00000584865.5:n.338_341delinsATCC
NM_000789.3:c.2392_2395delinsATCC	NP_000780.1:p.Ile798=
NM_001178057.1:c.670_673delinsATCC	NP_001171528.1:p.Ile224=
NM_152830.2:c.670_673delinsATCC	NP_690043.1:p.Ile224=
XM_005257110.1:c.1843_1846delinsATCC	XP_005257167.1:p.Ile615=
XM_006721737.2:c.730_733delinsATCC	XP_006721800.2:p.Ile244=
XM_006721737.3:c.730_733delinsATCC	XP_006721800.2:p.Ile244=
NM_000789.4:c.2392_2395delinsATCC MANE Select	NP_000780.1:p.Ile798=
NM_001178057.2:c.670_673delinsATCC	NP_001171528.1:p.Ile224=
NM_152830.3:c.670_673delinsATCC	NP_690043.1:p.Ile224=
NM_001382700.1:c.1825_1828delinsATCC	NP_001369629.1:p.Ile609=
NM_001382701.1:c.1540_1543delinsATCC	NP_001369630.1:p.Ile514=
NM_001382702.1:c.322_325delinsATCC	NP_001369631.1:p.Ile108=
NR_168483.1:n.770_773delinsATCC