Canonical Allele Identifier: CA2022884674

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209879_25209882delinsTCGA , CM000674.2:g.25209879_25209882delinsTCGA	GRCh38
NC_000012.11:g.25362813_25362816delinsTCGA , CM000674.1:g.25362813_25362816delinsTCGA	GRCh37
NC_000012.10:g.25254080_25254083delinsTCGA	NCBI36
NG_007524.1:g.46039_46042delinsTCGA
NG_007524.2:g.46122_46125delinsTCGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.141_144delinsTCGA	ENSP00000452512.1:p.Val47=
ENST00000685328.1:c.480_483delinsTCGA	ENSP00000508921.1:p.Val160=
ENST00000686877.1:c.*451_*454delinsTCGA	ENSP00000510431.1:n.*451_*454delinsTCGA
ENST00000687356.1:c.*178_*181delinsTCGA	ENSP00000510511.1:n.*178_*181delinsTCGA
ENST00000688228.1:n.954_957delinsTCGA
ENST00000688940.1:c.480_483delinsTCGA	ENSP00000509238.1:p.Val160=
ENST00000690406.1:c.283_286delinsTCGA
ENST00000690804.1:c.*441_*444delinsTCGA	ENSP00000508568.1:n.*441_*444delinsTCGA
ENST00000692768.1:c.282_285delinsTCGA	ENSP00000510254.1:p.Val94=
ENST00000693229.1:c.405_408delinsTCGA	ENSP00000509223.1:p.Val135=
ENST00000256078.10:c.*34_*37delinsTCGA MANE Plus Clinical	ENSP00000256078.5:n.*34_*37delinsTCGA
ENST00000311936.8:c.480_483delinsTCGA MANE Select	ENSP00000308495.3:p.Val160=
ENST00000256078.8:c.*34_*37delinsTCGA	ENSP00000256078.4:n.*34_*37delinsTCGA
ENST00000311936.7:c.480_483delinsTCGA	ENSP00000308495.3:p.Val160=
ENST00000557334.5:c.141_144delinsTCGA	ENSP00000452512.1:p.Val47=
NM_004985.4:c.480_483delinsTCGA	NP_004976.2:p.Val160=
NM_033360.3:c.*34_*37delinsTCGA	NP_203524.1:n.*34_*37delinsTCGA
XM_006719069.2:c.*34_*37delinsTCGA	XP_006719132.1:n.*34_*37delinsTCGA
XM_011520653.1:c.480_483delinsTCGA	XP_011518955.1:p.Val160=
XM_006719069.4:c.*34_*37delinsTCGA	XP_006719132.1:n.*34_*37delinsTCGA
XM_011520653.3:c.480_483delinsTCGA	XP_011518955.1:p.Val160=
NM_001369786.1:c.*34_*37delinsTCGA	NP_001356715.1:n.*34_*37delinsTCGA
NM_001369787.1:c.480_483delinsTCGA	NP_001356716.1:p.Val160=
NM_004985.5:c.480_483delinsTCGA MANE Select	NP_004976.2:p.Val160=
NM_033360.4:c.*34_*37delinsTCGA MANE Plus Clinical	NP_203524.1:n.*34_*37delinsTCGA