Canonical Allele Identifier: CA645572124

Gene: KRAS

Linked Data

• dbSNP Id: rs2135806216
• COSMIC: COSM513

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25245349_25245351delinsGCA , CM000674.2:g.25245349_25245351delinsGCA	GRCh38
NC_000012.11:g.25398283_25398285delinsGCA , CM000674.1:g.25398283_25398285delinsGCA	GRCh37
NC_000012.10:g.25289550_25289552delinsGCA	NCBI36
NG_007524.1:g.10570_10572delinsTGC
NG_007524.2:g.10653_10655delinsTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556131.2:c.34_36delinsTGC	ENSP00000451856.1:p.Gly12Cys
ENST00000557334.6:c.34_36delinsTGC	ENSP00000452512.1:p.Gly12Cys
ENST00000685328.1:c.34_36delinsTGC	ENSP00000508921.1:p.Gly12Cys
ENST00000686877.1:c.34_36delinsTGC	ENSP00000510431.1:p.Gly12Cys
ENST00000686969.1:c.34_36delinsTGC	ENSP00000510479.1:p.Gly12Cys
ENST00000687356.1:c.34_36delinsTGC	ENSP00000510511.1:p.Gly12Cys
ENST00000688940.1:c.34_36delinsTGC	ENSP00000509238.1:p.Gly12Cys
ENST00000690804.1:c.34_36delinsTGC	ENSP00000508568.1:p.Gly12Cys
ENST00000692768.1:c.-88+5400_-88+5402delinsTGC	ENSP00000510254.1:n.-88+5400_-88+5402delinsTGC
ENST00000693229.1:c.34_36delinsTGC	ENSP00000509223.1:p.Gly12Cys
ENST00000256078.10:c.34_36delinsTGC MANE Plus Clinical	ENSP00000256078.5:p.Gly12Cys
ENST00000311936.8:c.34_36delinsTGC MANE Select	ENSP00000308495.3:p.Gly12Cys
ENST00000256078.8:c.34_36delinsTGC	ENSP00000256078.4:p.Gly12Cys
ENST00000311936.7:c.34_36delinsTGC	ENSP00000308495.3:p.Gly12Cys
ENST00000556131.1:c.34_36delinsTGC	ENSP00000451856.1:p.Gly12Cys
ENST00000557334.5:c.34_36delinsTGC	ENSP00000452512.1:p.Gly12Cys
NM_004985.4:c.34_36delinsTGC	NP_004976.2:p.Gly12Cys
NM_033360.3:c.34_36delinsTGC	NP_203524.1:p.Gly12Cys
XM_006719069.2:c.34_36delinsTGC	XP_006719132.1:p.Gly12Cys
XM_011520653.1:c.34_36delinsTGC	XP_011518955.1:p.Gly12Cys
XM_006719069.4:c.34_36delinsTGC	XP_006719132.1:p.Gly12Cys
XM_011520653.3:c.34_36delinsTGC	XP_011518955.1:p.Gly12Cys
NM_001369786.1:c.34_36delinsTGC	NP_001356715.1:p.Gly12Cys
NM_001369787.1:c.34_36delinsTGC	NP_001356716.1:p.Gly12Cys
NM_004985.5:c.34_36delinsTGC MANE Select	NP_004976.2:p.Gly12Cys
NM_033360.4:c.34_36delinsTGC MANE Plus Clinical	NP_203524.1:p.Gly12Cys