Canonical Allele Identifier: CA2022897858

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25245152_25245157delinsGATAAC , CM000674.2:g.25245152_25245157delinsGATAAC	GRCh38
NC_000012.11:g.25398086_25398091delinsGATAAC , CM000674.1:g.25398086_25398091delinsGATAAC	GRCh37
NC_000012.10:g.25289353_25289358delinsGATAAC	NCBI36
NG_007524.1:g.10764_10769delinsGTTATC
NG_007524.2:g.10847_10852delinsGTTATC

Transcript Alleles

HGVS	Amino-acid change
ENST00000556131.2:c.111+117_111+122delinsGTTATC	ENSP00000451856.1:n.111+117_111+122delins...
ENST00000557334.6:c.111+117_111+122delinsGTTATC	ENSP00000452512.1:n.111+117_111+122delins...
ENST00000685328.1:c.111+117_111+122delinsGTTATC	ENSP00000508921.1:n.111+117_111+122delins...
ENST00000686877.1:c.111+117_111+122delinsGTTATC	ENSP00000510431.1:n.111+117_111+122delins...
ENST00000686969.1:c.111+117_111+122delinsGTTATC	ENSP00000510479.1:n.111+117_111+122delins...
ENST00000687356.1:c.111+117_111+122delinsGTTATC	ENSP00000510511.1:n.111+117_111+122delins...
ENST00000688940.1:c.111+117_111+122delinsGTTATC	ENSP00000509238.1:n.111+117_111+122delins...
ENST00000690804.1:c.111+117_111+122delinsGTTATC	ENSP00000508568.1:n.111+117_111+122delins...
ENST00000692768.1:c.-88+5594_-88+5599delinsGTTATC	ENSP00000510254.1:n.-88+5594_-88+5599deli...
ENST00000693229.1:c.111+117_111+122delinsGTTATC	ENSP00000509223.1:n.111+117_111+122delins...
ENST00000256078.10:c.111+117_111+122delinsGTTATC MANE Plus Clinical	ENSP00000256078.5:n.111+117_111+122delins...
ENST00000311936.8:c.111+117_111+122delinsGTTATC MANE Select	ENSP00000308495.3:n.111+117_111+122delins...
ENST00000256078.8:c.111+117_111+122delinsGTTATC	ENSP00000256078.4:n.111+117_111+122delins...
ENST00000311936.7:c.111+117_111+122delinsGTTATC	ENSP00000308495.3:n.111+117_111+122delins...
ENST00000556131.1:c.111+117_111+122delinsGTTATC	ENSP00000451856.1:n.111+117_111+122delins...
ENST00000557334.5:c.111+117_111+122delinsGTTATC	ENSP00000452512.1:n.111+117_111+122delins...
NM_004985.4:c.111+117_111+122delinsGTTATC	NP_004976.2:n.111+117_111+122delinsGTTATC...
NM_033360.3:c.111+117_111+122delinsGTTATC	NP_203524.1:n.111+117_111+122delinsGTTATC...
XM_006719069.2:c.111+117_111+122delinsGTTATC	XP_006719132.1:n.111+117_111+122delinsGTT...
XM_011520653.1:c.111+117_111+122delinsGTTATC	XP_011518955.1:n.111+117_111+122delinsGTT...
XM_006719069.4:c.111+117_111+122delinsGTTATC	XP_006719132.1:n.111+117_111+122delinsGTT...
XM_011520653.3:c.111+117_111+122delinsGTTATC	XP_011518955.1:n.111+117_111+122delinsGTT...
NM_001369786.1:c.111+117_111+122delinsGTTATC	NP_001356715.1:n.111+117_111+122delinsGTT...
NM_001369787.1:c.111+117_111+122delinsGTTATC	NP_001356716.1:n.111+117_111+122delinsGTT...
NM_004985.5:c.111+117_111+122delinsGTTATC MANE Select	NP_004976.2:n.111+117_111+122delinsGTTATC...
NM_033360.4:c.111+117_111+122delinsGTTATC MANE Plus Clinical	NP_203524.1:n.111+117_111+122delinsGTTATC...