Canonical Allele Identifier: CA2726048793

Gene: KRAS

Linked Data

• dbSNP Id: rs2141509269

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25227239del , CM000674.2:g.25227239del	GRCh38
NC_000012.11:g.25380173del , CM000674.1:g.25380173del	GRCh37
NC_000012.10:g.25271440del	NCBI36
NG_007524.1:g.28683del
NG_007524.2:g.28766del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-17327del	ENSP00000452512.1:n.112-17327del
ENST00000685328.1:c.286del	ENSP00000508921.1:p.Tyr96IlefsTer18
ENST00000686877.1:c.*257del	ENSP00000510431.1:n.*257del
ENST00000687356.1:c.112-1465del	ENSP00000510511.1:n.112-1465del
ENST00000688228.1:n.760del
ENST00000688940.1:c.286del	ENSP00000509238.1:p.Tyr96IlefsTer18
ENST00000690804.1:c.*247del	ENSP00000508568.1:n.*247del
ENST00000692768.1:c.88del	ENSP00000510254.1:p.Tyr30IlefsTer18
ENST00000693229.1:c.211del	ENSP00000509223.1:p.Tyr71IlefsTer18
ENST00000256078.10:c.286del MANE Plus Clinical	ENSP00000256078.5:p.Tyr96IlefsTer18
ENST00000311936.8:c.286del MANE Select	ENSP00000308495.3:p.Tyr96IlefsTer18
ENST00000256078.8:c.286del	ENSP00000256078.4:p.Tyr96IlefsTer18
ENST00000311936.7:c.286del	ENSP00000308495.3:p.Tyr96IlefsTer18
ENST00000557334.5:c.112-17327del	ENSP00000452512.1:n.112-17327del
NM_004985.4:c.286del	NP_004976.2:p.Tyr96IlefsTer18
NM_033360.3:c.286del	NP_203524.1:p.Tyr96IlefsTer18
XM_006719069.2:c.286del	XP_006719132.1:p.Tyr96IlefsTer18
XM_011520653.1:c.286del	XP_011518955.1:p.Tyr96IlefsTer18
XM_006719069.4:c.286del	XP_006719132.1:p.Tyr96IlefsTer18
XM_011520653.3:c.286del	XP_011518955.1:p.Tyr96IlefsTer18
NM_001369786.1:c.286del	NP_001356715.1:p.Tyr96IlefsTer18
NM_001369787.1:c.286del	NP_001356716.1:p.Tyr96IlefsTer18
NM_004985.5:c.286del MANE Select	NP_004976.2:p.Tyr96IlefsTer18
NM_033360.4:c.286del MANE Plus Clinical	NP_203524.1:p.Tyr96IlefsTer18