Canonical Allele Identifier: CA2022884477

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209768_25209769delinsGC , CM000674.2:g.25209768_25209769delinsGC	GRCh38
NC_000012.11:g.25362702_25362703delinsGC , CM000674.1:g.25362702_25362703delinsGC	GRCh37
NC_000012.10:g.25253969_25253970delinsGC	NCBI36
NG_007524.1:g.46152_46153delinsGC
NG_007524.2:g.46235_46236delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*26_*27delinsGC	ENSP00000452512.1:n.*26_*27delinsGC
ENST00000685328.1:c.*26_*27delinsGC	ENSP00000508921.1:n.*26_*27delinsGC
ENST00000686877.1:c.*564_*565delinsGC	ENSP00000510431.1:n.*564_*565delinsGC
ENST00000687356.1:c.*291_*292delinsGC	ENSP00000510511.1:n.*291_*292delinsGC
ENST00000688228.1:n.1067_1068delinsGC
ENST00000688940.1:c.*26_*27delinsGC	ENSP00000509238.1:n.*26_*27delinsGC
ENST00000690406.1:c.396_397delinsGC
ENST00000690804.1:c.*554_*555delinsGC	ENSP00000508568.1:n.*554_*555delinsGC
ENST00000692768.1:c.*26_*27delinsGC	ENSP00000510254.1:n.*26_*27delinsGC
ENST00000693229.1:c.*26_*27delinsGC	ENSP00000509223.1:n.*26_*27delinsGC
ENST00000256078.10:c.*147_*148delinsGC MANE Plus Clinical	ENSP00000256078.5:n.*147_*148delinsGC
ENST00000311936.8:c.*26_*27delinsGC MANE Select	ENSP00000308495.3:n.*26_*27delinsGC
ENST00000256078.8:c.*147_*148delinsGC	ENSP00000256078.4:n.*147_*148delinsGC
ENST00000311936.7:c.*26_*27delinsGC	ENSP00000308495.3:n.*26_*27delinsGC
ENST00000557334.5:c.*26_*27delinsGC	ENSP00000452512.1:n.*26_*27delinsGC
NM_004985.4:c.*26_*27delinsGC	NP_004976.2:n.*26_*27delinsGC
NM_033360.3:c.*147_*148delinsGC	NP_203524.1:n.*147_*148delinsGC
XM_011520653.1:c.*26_*27delinsGC	XP_011518955.1:n.*26_*27delinsGC
XM_011520653.3:c.*26_*27delinsGC	XP_011518955.1:n.*26_*27delinsGC
NM_001369786.1:c.*147_*148delinsGC	NP_001356715.1:n.*147_*148delinsGC
NM_001369787.1:c.*26_*27delinsGC	NP_001356716.1:n.*26_*27delinsGC
NM_004985.5:c.*26_*27delinsGC MANE Select	NP_004976.2:n.*26_*27delinsGC
NM_033360.4:c.*147_*148delinsGC MANE Plus Clinical	NP_203524.1:n.*147_*148delinsGC