Canonical Allele Identifier: CA2022884558
Gene: KRAS HGNC NCBI

Linked Data

dbSNP Id: rs1951183686

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209825_25209828del , CM000674.2:g.25209825_25209828del GRCh38
NC_000012.11:g.25362759_25362762del , CM000674.1:g.25362759_25362762del GRCh37
NC_000012.10:g.25254026_25254029del NCBI36
NG_007524.1:g.46095_46098del
NG_007524.2:g.46178_46181del

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.197_200del ENSP00000452512.1:p.Lys66SerfsTer7
ENST00000685328.1:c.536_539del ENSP00000508921.1:p.Lys179SerfsTer7
ENST00000686877.1:c.*507_*510del ENSP00000510431.1:n.*507_*510del
ENST00000687356.1:c.*234_*237del ENSP00000510511.1:n.*234_*237del
ENST00000688228.1:n.1010_1013del
ENST00000688940.1:c.536_539del ENSP00000509238.1:p.Lys179SerfsTer7
ENST00000690406.1:c.339_342del
ENST00000690804.1:c.*497_*500del ENSP00000508568.1:n.*497_*500del
ENST00000692768.1:c.338_341del ENSP00000510254.1:p.Lys113SerfsTer7
ENST00000693229.1:c.461_464del ENSP00000509223.1:p.Lys154SerfsTer7
ENST00000256078.10:c.*90_*93del MANE Plus Clinical ENSP00000256078.5:n.*90_*93del
ENST00000311936.8:c.536_539del MANE Select ENSP00000308495.3:p.Lys179SerfsTer7
ENST00000256078.8:c.*90_*93del ENSP00000256078.4:n.*90_*93del
ENST00000311936.7:c.536_539del ENSP00000308495.3:p.Lys179SerfsTer7
ENST00000557334.5:c.197_200del ENSP00000452512.1:p.Lys66SerfsTer7
NM_004985.4:c.536_539del NP_004976.2:p.Lys179SerfsTer7
NM_033360.3:c.*90_*93del NP_203524.1:n.*90_*93del
XM_011520653.1:c.536_539del XP_011518955.1:p.Lys179SerfsTer7
XM_011520653.3:c.536_539del XP_011518955.1:p.Lys179SerfsTer7
NM_001369786.1:c.*90_*93del NP_001356715.1:n.*90_*93del
NM_001369787.1:c.536_539del NP_001356716.1:p.Lys179SerfsTer7
NM_004985.5:c.536_539del MANE Select NP_004976.2:p.Lys179SerfsTer7
NM_033360.4:c.*90_*93del MANE Plus Clinical NP_203524.1:n.*90_*93del