Canonical Allele Identifier: CA645572098

Gene: KRAS

Linked Data

• ClinVar Variation Id: 3116215
• ClinVar RCV Id: RCV004412079
• dbSNP Id: rs2141510126
• COSMIC: COSM87298 ; COSM4387500

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25227343_25227344delinsTT , CM000674.2:g.25227343_25227344delinsTT	GRCh38
NC_000012.11:g.25380277_25380278delinsTT , CM000674.1:g.25380277_25380278delinsTT	GRCh37
NC_000012.10:g.25271544_25271545delinsTT	NCBI36
NG_007524.1:g.28577_28578delinsAA
NG_007524.2:g.28660_28661delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-17433_112-17432delinsAA	ENSP00000452512.1:n.112-17433_112-17432delinsAA
ENST00000685328.1:c.180_181delinsAA	ENSP00000508921.1:p.Gln61Lys
ENST00000686877.1:c.*151_*152delinsAA	ENSP00000510431.1:n.*151_*152delinsAA
ENST00000687356.1:c.112-1571_112-1570delinsAA	ENSP00000510511.1:n.112-1571_112-1570delinsAA
ENST00000688228.1:n.654_655delinsAA
ENST00000688940.1:c.180_181delinsAA	ENSP00000509238.1:p.Gln61Lys
ENST00000690804.1:c.*141_*142delinsAA	ENSP00000508568.1:n.*141_*142delinsAA
ENST00000692768.1:c.-19_-18delinsAA	ENSP00000510254.1:n.-19_-18delinsAA
ENST00000693229.1:c.112-7_112-6delinsAA	ENSP00000509223.1:n.112-7_112-6delinsAA
ENST00000256078.10:c.180_181delinsAA MANE Plus Clinical	ENSP00000256078.5:p.Gln61Lys
ENST00000311936.8:c.180_181delinsAA MANE Select	ENSP00000308495.3:p.Gln61Lys
ENST00000256078.8:c.180_181delinsAA	ENSP00000256078.4:p.Gln61Lys
ENST00000311936.7:c.180_181delinsAA	ENSP00000308495.3:p.Gln61Lys
ENST00000557334.5:c.112-17433_112-17432delinsAA	ENSP00000452512.1:n.112-17433_112-17432delinsAA
NM_004985.4:c.180_181delinsAA	NP_004976.2:p.Gln61Lys
NM_033360.3:c.180_181delinsAA	NP_203524.1:p.Gln61Lys
XM_006719069.2:c.180_181delinsAA	XP_006719132.1:p.Gln61Lys
XM_011520653.1:c.180_181delinsAA	XP_011518955.1:p.Gln61Lys
XM_006719069.4:c.180_181delinsAA	XP_006719132.1:p.Gln61Lys
XM_011520653.3:c.180_181delinsAA	XP_011518955.1:p.Gln61Lys
NM_001369786.1:c.180_181delinsAA	NP_001356715.1:p.Gln61Lys
NM_001369787.1:c.180_181delinsAA	NP_001356716.1:p.Gln61Lys
NM_004985.5:c.180_181delinsAA MANE Select	NP_004976.2:p.Gln61Lys
NM_033360.4:c.180_181delinsAA MANE Plus Clinical	NP_203524.1:p.Gln61Lys