Canonical Allele Identifier: CA645572086
Gene: KRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25225626_25225627insA , CM000674.2:g.25225626_25225627insA GRCh38
NC_000012.11:g.25378560_25378561insA , CM000674.1:g.25378560_25378561insA GRCh37
NC_000012.10:g.25269827_25269828insA NCBI36
NG_007524.1:g.30294_30295insT
NG_007524.2:g.30377_30378insT

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.112-15716_112-15715insT ENSP00000452512.1:n.112-15716_112-15715in...
ENST00000685328.1:c.437_438insT ENSP00000508921.1:p.Thr148AspfsTer6
ENST00000686877.1:c.*408_*409insT ENSP00000510431.1:n.*408_*409insT
ENST00000687356.1:c.*135_*136insT ENSP00000510511.1:n.*135_*136insT
ENST00000688228.1:n.911_912insT
ENST00000688940.1:c.437_438insT ENSP00000509238.1:p.Thr148AspfsTer6
ENST00000690406.1:c.147_148insT
ENST00000690804.1:c.*398_*399insT ENSP00000508568.1:n.*398_*399insT
ENST00000692768.1:c.239_240insT ENSP00000510254.1:p.Thr82AspfsTer6
ENST00000693229.1:c.362_363insT ENSP00000509223.1:p.Thr123AspfsTer6
ENST00000256078.10:c.437_438insT MANE Plus Clinical ENSP00000256078.5:p.Thr148AspfsTer?
ENST00000311936.8:c.437_438insT MANE Select ENSP00000308495.3:p.Thr148AspfsTer6
ENST00000256078.8:c.437_438insT ENSP00000256078.4:p.Thr148AspfsTer?
ENST00000311936.7:c.437_438insT ENSP00000308495.3:p.Thr148AspfsTer6
ENST00000557334.5:c.112-15716_112-15715insT ENSP00000452512.1:n.112-15716_112-15715in...
NM_004985.4:c.437_438insT NP_004976.2:p.Thr148AspfsTer6
NM_033360.3:c.437_438insT NP_203524.1:p.Thr148AspfsTer?
XM_006719069.2:c.437_438insT XP_006719132.1:p.Thr148AspfsTer?
XM_011520653.1:c.437_438insT XP_011518955.1:p.Thr148AspfsTer6
XM_006719069.4:c.437_438insT XP_006719132.1:p.Thr148AspfsTer?
XM_011520653.3:c.437_438insT XP_011518955.1:p.Thr148AspfsTer6
NM_001369786.1:c.437_438insT NP_001356715.1:p.Thr148AspfsTer?
NM_001369787.1:c.437_438insT NP_001356716.1:p.Thr148AspfsTer6
NM_004985.5:c.437_438insT MANE Select NP_004976.2:p.Thr148AspfsTer6
NM_033360.4:c.437_438insT MANE Plus Clinical NP_203524.1:p.Thr148AspfsTer?