Canonical Allele Identifier: CA912973924
Gene: KRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25225689_25225690insTCAACCGGTTTGCGGCCCATTTTATTAATCAGGCGGCGGGCAACCGGTCCGCCGATCAGACCGCCGAACACCAG , CM000674.2:g.25225689_25225690insTCAACCGGTTTGCGGCCCATTTTATTAATCAGGCGGCGGGCAACCGGTCCGCCGATCAGACCGCCGAACACCAG GRCh38
NC_000012.11:g.25378623_25378624insTCAACCGGTTTGCGGCCCATTTTATTAATCAGGCGGCGGGCAACCGGTCCGCCGATCAGACCGCCGAACACCAG , CM000674.1:g.25378623_25378624insTCAACCGGTTTGCGGCCCATTTTATTAATCAGGCGGCGGGCAACCGGTCCGCCGATCAGACCGCCGAACACCAG GRCh37
NC_000012.10:g.25269890_25269891insTCAACCGGTTTGCGGCCCATTTTATTAATCAGGCGGCGGGCAACCGGTCCGCCGATCAGACCGCCGAACACCAG NCBI36
NG_007524.1:g.30231_30232insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA
NG_007524.2:g.30314_30315insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000557334.6:c.112-15779_112-15778insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA ENSP00000452512.1:n.112-15779_112-15778insCTGGTGTTCGGCGGTCTGA...
ENST00000685328.1:c.374_375insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA ENSP00000508921.1:p.Asp126TrpfsTer6
ENST00000686877.1:c.*345_*346insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA ENSP00000510431.1:n.*345_*346insCTGGTGTTCGGCGGTCTGATCGGCGGACC...
ENST00000687356.1:c.*72_*73insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA ENSP00000510511.1:n.*72_*73insCTGGTGTTCGGCGGTCTGATCGGCGGACCGG...
ENST00000688228.1:n.848_849insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA
ENST00000688940.1:c.374_375insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA ENSP00000509238.1:p.Asp126TrpfsTer6
ENST00000690406.1:c.84_85insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA
ENST00000690804.1:c.*335_*336insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA ENSP00000508568.1:n.*335_*336insCTGGTGTTCGGCGGTCTGATCGGCGGACC...
ENST00000692768.1:c.176_177insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA ENSP00000510254.1:p.Asp60TrpfsTer6
ENST00000693229.1:c.299_300insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA ENSP00000509223.1:p.Asp101TrpfsTer6
ENST00000256078.10:c.374_375insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA MANE Plus Clinical ENSP00000256078.5:p.Asp126TrpfsTer6
ENST00000311936.8:c.374_375insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA MANE Select ENSP00000308495.3:p.Asp126TrpfsTer6
ENST00000256078.8:c.374_375insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA ENSP00000256078.4:p.Asp126TrpfsTer6
ENST00000311936.7:c.374_375insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA ENSP00000308495.3:p.Asp126TrpfsTer6
ENST00000557334.5:c.112-15779_112-15778insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA ENSP00000452512.1:n.112-15779_112-15778insCTGGTGTTCGGCGGTCTGA...
NM_004985.4:c.374_375insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA NP_004976.2:p.Asp126TrpfsTer6
NM_033360.3:c.374_375insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA NP_203524.1:p.Asp126TrpfsTer6
XM_006719069.2:c.374_375insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA XP_006719132.1:p.Asp126TrpfsTer6
XM_011520653.1:c.374_375insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA XP_011518955.1:p.Asp126TrpfsTer6
XM_006719069.4:c.374_375insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA XP_006719132.1:p.Asp126TrpfsTer6
XM_011520653.3:c.374_375insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA XP_011518955.1:p.Asp126TrpfsTer6
NM_001369786.1:c.374_375insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA NP_001356715.1:p.Asp126TrpfsTer6
NM_001369787.1:c.374_375insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA NP_001356716.1:p.Asp126TrpfsTer6
NM_004985.5:c.374_375insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA MANE Select NP_004976.2:p.Asp126TrpfsTer6
NM_033360.4:c.374_375insCTGGTGTTCGGCGGTCTGATCGGCGGACCGGTTGCCCGCCGCCTGATTAATAAAATGGGCCGCAAACCGGTTGA MANE Plus Clinical NP_203524.1:p.Asp126TrpfsTer6