Canonical Allele Identifier: CA2022905563
Gene: KRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25225450_25225458delinsGACACTGGA , CM000674.2:g.25225450_25225458delinsGACACTGGA GRCh38
NC_000012.11:g.25378384_25378392delinsGACACTGGA , CM000674.1:g.25378384_25378392delinsGACACTGGA GRCh37
NC_000012.10:g.25269651_25269659delinsGACACTGGA NCBI36
NG_007524.1:g.30463_30471delinsTCCAGTGTC
NG_007524.2:g.30546_30554delinsTCCAGTGTC

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.112-15547_112-15539delinsTCCAGTGTC ENSP00000452512.1:n.112-15547_112-15539de...
ENST00000685328.1:c.450+156_450+164delinsTCCAGTGTC ENSP00000508921.1:n.450+156_450+164delins...
ENST00000686877.1:c.*421+156_*421+164delinsTCCAGTGTC ENSP00000510431.1:n.*421+156_*421+164deli...
ENST00000687356.1:c.*148+156_*148+164delinsTCCAGTGTC ENSP00000510511.1:n.*148+156_*148+164deli...
ENST00000688228.1:n.924+156_924+164delinsTCCAGTGTC
ENST00000688940.1:c.450+156_450+164delinsTCCAGTGTC ENSP00000509238.1:n.450+156_450+164delins...
ENST00000690406.1:c.160+156_160+164delinsTCCAGTGTC
ENST00000690804.1:c.*411+156_*411+164delinsTCCAGTGTC ENSP00000508568.1:n.*411+156_*411+164deli...
ENST00000692768.1:c.252+156_252+164delinsTCCAGTGTC ENSP00000510254.1:n.252+156_252+164delins...
ENST00000693229.1:c.375+156_375+164delinsTCCAGTGTC ENSP00000509223.1:n.375+156_375+164delins...
ENST00000256078.10:c.450+156_450+164delinsTCCAGTGTC MANE Plus Clinical ENSP00000256078.5:n.450+156_450+164delins...
ENST00000311936.8:c.450+156_450+164delinsTCCAGTGTC MANE Select ENSP00000308495.3:n.450+156_450+164delins...
ENST00000256078.8:c.450+156_450+164delinsTCCAGTGTC ENSP00000256078.4:n.450+156_450+164delins...
ENST00000311936.7:c.450+156_450+164delinsTCCAGTGTC ENSP00000308495.3:n.450+156_450+164delins...
ENST00000557334.5:c.112-15547_112-15539delinsTCCAGTGTC ENSP00000452512.1:n.112-15547_112-15539de...
NM_004985.4:c.450+156_450+164delinsTCCAGTGTC NP_004976.2:n.450+156_450+164delinsTCCAGT...
NM_033360.3:c.450+156_450+164delinsTCCAGTGTC NP_203524.1:n.450+156_450+164delinsTCCAGT...
XM_006719069.2:c.450+156_450+164delinsTCCAGTGTC XP_006719132.1:n.450+156_450+164delinsTCC...
XM_011520653.1:c.450+156_450+164delinsTCCAGTGTC XP_011518955.1:n.450+156_450+164delinsTCC...
XM_006719069.4:c.450+156_450+164delinsTCCAGTGTC XP_006719132.1:n.450+156_450+164delinsTCC...
XM_011520653.3:c.450+156_450+164delinsTCCAGTGTC XP_011518955.1:n.450+156_450+164delinsTCC...
NM_001369786.1:c.450+156_450+164delinsTCCAGTGTC NP_001356715.1:n.450+156_450+164delinsTCC...
NM_001369787.1:c.450+156_450+164delinsTCCAGTGTC NP_001356716.1:n.450+156_450+164delinsTCC...
NM_004985.5:c.450+156_450+164delinsTCCAGTGTC MANE Select NP_004976.2:n.450+156_450+164delinsTCCAGT...
NM_033360.4:c.450+156_450+164delinsTCCAGTGTC MANE Plus Clinical NP_203524.1:n.450+156_450+164delinsTCCAGT...