Canonical Allele Identifier: CA2022906154

Gene: KRAS

Linked Data

• ClinVar Variation Id: 1046139
• ClinVar RCV Id: RCV001350656 ; RCV002499701
• dbSNP Id: rs1951383854

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225675_25225676delinsAT , CM000674.2:g.25225675_25225676delinsAT	GRCh38
NC_000012.11:g.25378609_25378610delinsAT , CM000674.1:g.25378609_25378610delinsAT	GRCh37
NC_000012.10:g.25269876_25269877delinsAT	NCBI36
NG_007524.1:g.30245_30246delinsAT
NG_007524.2:g.30328_30329delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15765_112-15764delinsAT	ENSP00000452512.1:n.112-15765_112-15764delinsAT
ENST00000685328.1:c.388_389delinsAT	ENSP00000508921.1:p.Ala130Ile
ENST00000686877.1:c.*359_*360delinsAT	ENSP00000510431.1:n.*359_*360delinsAT
ENST00000687356.1:c.*86_*87delinsAT	ENSP00000510511.1:n.*86_*87delinsAT
ENST00000688228.1:n.862_863delinsAT
ENST00000688940.1:c.388_389delinsAT	ENSP00000509238.1:p.Ala130Ile
ENST00000690406.1:c.98_99delinsAT
ENST00000690804.1:c.*349_*350delinsAT	ENSP00000508568.1:n.*349_*350delinsAT
ENST00000692768.1:c.190_191delinsAT	ENSP00000510254.1:p.Ala64Ile
ENST00000693229.1:c.313_314delinsAT	ENSP00000509223.1:p.Ala105Ile
ENST00000256078.10:c.388_389delinsAT MANE Plus Clinical	ENSP00000256078.5:p.Ala130Ile
ENST00000311936.8:c.388_389delinsAT MANE Select	ENSP00000308495.3:p.Ala130Ile
ENST00000256078.8:c.388_389delinsAT	ENSP00000256078.4:p.Ala130Ile
ENST00000311936.7:c.388_389delinsAT	ENSP00000308495.3:p.Ala130Ile
ENST00000557334.5:c.112-15765_112-15764delinsAT	ENSP00000452512.1:n.112-15765_112-15764delinsAT
NM_004985.4:c.388_389delinsAT	NP_004976.2:p.Ala130Ile
NM_033360.3:c.388_389delinsAT	NP_203524.1:p.Ala130Ile
XM_006719069.2:c.388_389delinsAT	XP_006719132.1:p.Ala130Ile
XM_011520653.1:c.388_389delinsAT	XP_011518955.1:p.Ala130Ile
XM_006719069.4:c.388_389delinsAT	XP_006719132.1:p.Ala130Ile
XM_011520653.3:c.388_389delinsAT	XP_011518955.1:p.Ala130Ile
NM_001369786.1:c.388_389delinsAT	NP_001356715.1:p.Ala130Ile
NM_001369787.1:c.388_389delinsAT	NP_001356716.1:p.Ala130Ile
NM_004985.5:c.388_389delinsAT MANE Select	NP_004976.2:p.Ala130Ile
NM_033360.4:c.388_389delinsAT MANE Plus Clinical	NP_203524.1:p.Ala130Ile