Canonical Allele Identifier: CA2022884656
Gene: KRAS HGNC NCBI

Linked Data

dbSNP Id: rs1951184389

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209872_25209877del , CM000674.2:g.25209872_25209877del GRCh38
NC_000012.11:g.25362806_25362811del , CM000674.1:g.25362806_25362811del GRCh37
NC_000012.10:g.25254073_25254078del NCBI36
NG_007524.1:g.46044_46049del
NG_007524.2:g.46127_46132del

Transcript Alleles

HGVS Amino-acid Change
ENST00000557334.6:c.146_151del ENSP00000452512.1:p.Glu49_Arg51delinsGly
ENST00000685328.1:c.485_490del ENSP00000508921.1:p.Glu162_Arg164delinsGly
ENST00000686877.1:c.*456_*461del ENSP00000510431.1:n.*456_*461del
ENST00000687356.1:c.*183_*188del ENSP00000510511.1:n.*183_*188del
ENST00000688228.1:n.959_964del
ENST00000688940.1:c.485_490del ENSP00000509238.1:p.Glu162_Arg164delinsGly
ENST00000690406.1:c.288_293del
ENST00000690804.1:c.*446_*451del ENSP00000508568.1:n.*446_*451del
ENST00000692768.1:c.287_292del ENSP00000510254.1:p.Glu96_Arg98delinsGly
ENST00000693229.1:c.410_415del ENSP00000509223.1:p.Glu137_Arg139delinsGly
ENST00000256078.10:c.*39_*44del MANE Plus Clinical ENSP00000256078.5:n.*39_*44del
ENST00000311936.8:c.485_490del MANE Select ENSP00000308495.3:p.Glu162_Arg164delinsGly
ENST00000256078.8:c.*39_*44del ENSP00000256078.4:n.*39_*44del
ENST00000311936.7:c.485_490del ENSP00000308495.3:p.Glu162_Arg164delinsGly
ENST00000557334.5:c.146_151del ENSP00000452512.1:p.Glu49_Arg51delinsGly
NM_004985.4:c.485_490del NP_004976.2:p.Glu162_Arg164delinsGly
NM_033360.3:c.*39_*44del NP_203524.1:n.*39_*44del
XM_006719069.2:c.*39_*44del XP_006719132.1:n.*39_*44del
XM_011520653.1:c.485_490del XP_011518955.1:p.Glu162_Arg164delinsGly
XM_006719069.4:c.*39_*44del XP_006719132.1:n.*39_*44del
XM_011520653.3:c.485_490del XP_011518955.1:p.Glu162_Arg164delinsGly
NM_001369786.1:c.*39_*44del NP_001356715.1:n.*39_*44del
NM_001369787.1:c.485_490del NP_001356716.1:p.Glu162_Arg164delinsGly
NM_004985.5:c.485_490del MANE Select NP_004976.2:p.Glu162_Arg164delinsGly
NM_033360.4:c.*39_*44del MANE Plus Clinical NP_203524.1:n.*39_*44del