Canonical Allele Identifier: CA2978503607

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225628_25225632del , CM000674.2:g.25225628_25225632del	GRCh38
NC_000012.11:g.25378562_25378566del , CM000674.1:g.25378562_25378566del	GRCh37
NC_000012.10:g.25269829_25269833del	NCBI36
NG_007524.1:g.30289_30293del
NG_007524.2:g.30372_30376del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15721_112-15717del	ENSP00000452512.1:n.112-15721_112-15717del
ENST00000685328.1:c.432_436del	ENSP00000508921.1:p.Ser145LysfsTer7
ENST00000686877.1:c.*403_*407del	ENSP00000510431.1:n.*403_*407del
ENST00000687356.1:c.*130_*134del	ENSP00000510511.1:n.*130_*134del
ENST00000688228.1:n.906_910del
ENST00000688940.1:c.432_436del	ENSP00000509238.1:p.Ser145LysfsTer7
ENST00000690406.1:c.142_146del
ENST00000690804.1:c.*393_*397del	ENSP00000508568.1:n.*393_*397del
ENST00000692768.1:c.234_238del	ENSP00000510254.1:p.Ser79LysfsTer7
ENST00000693229.1:c.357_361del	ENSP00000509223.1:p.Ser120LysfsTer7
ENST00000256078.10:c.432_436del MANE Plus Clinical	ENSP00000256078.5:p.Ser145LysfsTer?
ENST00000311936.8:c.432_436del MANE Select	ENSP00000308495.3:p.Ser145LysfsTer7
ENST00000256078.8:c.432_436del	ENSP00000256078.4:p.Ser145LysfsTer?
ENST00000311936.7:c.432_436del	ENSP00000308495.3:p.Ser145LysfsTer7
ENST00000557334.5:c.112-15721_112-15717del	ENSP00000452512.1:n.112-15721_112-15717del
NM_004985.4:c.432_436del	NP_004976.2:p.Ser145LysfsTer7
NM_033360.3:c.432_436del	NP_203524.1:p.Ser145LysfsTer?
XM_006719069.2:c.432_436del	XP_006719132.1:p.Ser145LysfsTer?
XM_011520653.1:c.432_436del	XP_011518955.1:p.Ser145LysfsTer7
XM_006719069.4:c.432_436del	XP_006719132.1:p.Ser145LysfsTer?
XM_011520653.3:c.432_436del	XP_011518955.1:p.Ser145LysfsTer7
NM_001369786.1:c.432_436del	NP_001356715.1:p.Ser145LysfsTer?
NM_001369787.1:c.432_436del	NP_001356716.1:p.Ser145LysfsTer7
NM_004985.5:c.432_436del MANE Select	NP_004976.2:p.Ser145LysfsTer7
NM_033360.4:c.432_436del MANE Plus Clinical	NP_203524.1:p.Ser145LysfsTer?