Canonical Allele Identifier: CA2022906157

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225675_25225676delinsGC , CM000674.2:g.25225675_25225676delinsGC	GRCh38
NC_000012.11:g.25378609_25378610delinsGC , CM000674.1:g.25378609_25378610delinsGC	GRCh37
NC_000012.10:g.25269876_25269877delinsGC	NCBI36
NG_007524.1:g.30245_30246delinsGC
NG_007524.2:g.30328_30329delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15765_112-15764delinsGC	ENSP00000452512.1:n.112-15765_112-15764delinsGC
ENST00000685328.1:c.388_389delinsGC	ENSP00000508921.1:p.Ala130=
ENST00000686877.1:c.*359_*360delinsGC	ENSP00000510431.1:n.*359_*360delinsGC
ENST00000687356.1:c.*86_*87delinsGC	ENSP00000510511.1:n.*86_*87delinsGC
ENST00000688228.1:n.862_863delinsGC
ENST00000688940.1:c.388_389delinsGC	ENSP00000509238.1:p.Ala130=
ENST00000690406.1:c.98_99delinsGC
ENST00000690804.1:c.*349_*350delinsGC	ENSP00000508568.1:n.*349_*350delinsGC
ENST00000692768.1:c.190_191delinsGC	ENSP00000510254.1:p.Ala64=
ENST00000693229.1:c.313_314delinsGC	ENSP00000509223.1:p.Ala105=
ENST00000256078.10:c.388_389delinsGC MANE Plus Clinical	ENSP00000256078.5:p.Ala130=
ENST00000311936.8:c.388_389delinsGC MANE Select	ENSP00000308495.3:p.Ala130=
ENST00000256078.8:c.388_389delinsGC	ENSP00000256078.4:p.Ala130=
ENST00000311936.7:c.388_389delinsGC	ENSP00000308495.3:p.Ala130=
ENST00000557334.5:c.112-15765_112-15764delinsGC	ENSP00000452512.1:n.112-15765_112-15764delinsGC
NM_004985.4:c.388_389delinsGC	NP_004976.2:p.Ala130=
NM_033360.3:c.388_389delinsGC	NP_203524.1:p.Ala130=
XM_006719069.2:c.388_389delinsGC	XP_006719132.1:p.Ala130=
XM_011520653.1:c.388_389delinsGC	XP_011518955.1:p.Ala130=
XM_006719069.4:c.388_389delinsGC	XP_006719132.1:p.Ala130=
XM_011520653.3:c.388_389delinsGC	XP_011518955.1:p.Ala130=
NM_001369786.1:c.388_389delinsGC	NP_001356715.1:p.Ala130=
NM_001369787.1:c.388_389delinsGC	NP_001356716.1:p.Ala130=
NM_004985.5:c.388_389delinsGC MANE Select	NP_004976.2:p.Ala130=
NM_033360.4:c.388_389delinsGC MANE Plus Clinical	NP_203524.1:p.Ala130=