Canonical Allele Identifier: CA645572105

Gene: KRAS

Linked Data

• COSMIC: COSM219781 ; COSM6022434

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25245346_25245348dup , CM000674.2:g.25245346_25245348dup	GRCh38
NC_000012.11:g.25398280_25398282dup , CM000674.1:g.25398280_25398282dup	GRCh37
NC_000012.10:g.25289547_25289549dup	NCBI36
NG_007524.1:g.10574_10576dup
NG_007524.2:g.10657_10659dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000556131.2:c.38_40dup	ENSP00000451856.1:p.Gly13_Val14insGly
ENST00000557334.6:c.38_40dup	ENSP00000452512.1:p.Gly13_Val14insGly
ENST00000685328.1:c.38_40dup	ENSP00000508921.1:p.Gly13_Val14insGly
ENST00000686877.1:c.38_40dup	ENSP00000510431.1:p.Gly13_Val14insGly
ENST00000686969.1:c.38_40dup	ENSP00000510479.1:p.Gly13_Val14insGly
ENST00000687356.1:c.38_40dup	ENSP00000510511.1:p.Gly13_Val14insGly
ENST00000688940.1:c.38_40dup	ENSP00000509238.1:p.Gly13_Val14insGly
ENST00000690804.1:c.38_40dup	ENSP00000508568.1:p.Gly13_Val14insGly
ENST00000692768.1:c.-88+5404_-88+5406dup	ENSP00000510254.1:n.-88+5404_-88+5406dup
ENST00000693229.1:c.38_40dup	ENSP00000509223.1:p.Gly13_Val14insGly
ENST00000256078.10:c.38_40dup MANE Plus Clinical	ENSP00000256078.5:p.Gly13_Val14insGly
ENST00000311936.8:c.38_40dup MANE Select	ENSP00000308495.3:p.Gly13_Val14insGly
ENST00000256078.8:c.38_40dup	ENSP00000256078.4:p.Gly13_Val14insGly
ENST00000311936.7:c.38_40dup	ENSP00000308495.3:p.Gly13_Val14insGly
ENST00000556131.1:c.38_40dup	ENSP00000451856.1:p.Gly13_Val14insGly
ENST00000557334.5:c.38_40dup	ENSP00000452512.1:p.Gly13_Val14insGly
NM_004985.4:c.38_40dup	NP_004976.2:p.Gly13_Val14insGly
NM_033360.3:c.38_40dup	NP_203524.1:p.Gly13_Val14insGly
XM_006719069.2:c.38_40dup	XP_006719132.1:p.Gly13_Val14insGly
XM_011520653.1:c.38_40dup	XP_011518955.1:p.Gly13_Val14insGly
XM_006719069.4:c.38_40dup	XP_006719132.1:p.Gly13_Val14insGly
XM_011520653.3:c.38_40dup	XP_011518955.1:p.Gly13_Val14insGly
NM_001369786.1:c.38_40dup	NP_001356715.1:p.Gly13_Val14insGly
NM_001369787.1:c.38_40dup	NP_001356716.1:p.Gly13_Val14insGly
NM_004985.5:c.38_40dup MANE Select	NP_004976.2:p.Gly13_Val14insGly
NM_033360.4:c.38_40dup MANE Plus Clinical	NP_203524.1:p.Gly13_Val14insGly