Canonical Allele Identifier: CA2580085347

Gene: KRAS

Linked Data

• ClinVar Variation Id: 1710999
• ClinVar RCV Id: RCV002292286

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25245402_25245403insG , CM000674.2:g.25245402_25245403insG	GRCh38
NC_000012.11:g.25398336_25398337insG , CM000674.1:g.25398336_25398337insG	GRCh37
NC_000012.10:g.25289603_25289604insG	NCBI36
NG_007524.1:g.10518_10519insC
NG_007524.2:g.10601_10602insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556131.2:c.-11-8_-11-7insC	ENSP00000451856.1:n.-11-8_-11-7insC
ENST00000557334.6:c.-11-8_-11-7insC	ENSP00000452512.1:n.-11-8_-11-7insC
ENST00000685328.1:c.-11-8_-11-7insC	ENSP00000508921.1:n.-11-8_-11-7insC
ENST00000686877.1:c.-11-8_-11-7insC	ENSP00000510431.1:n.-11-8_-11-7insC
ENST00000686969.1:c.-11-8_-11-7insC	ENSP00000510479.1:n.-11-8_-11-7insC
ENST00000687356.1:c.-11-8_-11-7insC	ENSP00000510511.1:n.-11-8_-11-7insC
ENST00000688940.1:c.-11-8_-11-7insC	ENSP00000509238.1:n.-11-8_-11-7insC
ENST00000690804.1:c.-11-8_-11-7insC	ENSP00000508568.1:n.-11-8_-11-7insC
ENST00000692768.1:c.-88+5348_-88+5349insC	ENSP00000510254.1:n.-88+5348_-88+5349insC
ENST00000693229.1:c.-11-8_-11-7insC	ENSP00000509223.1:n.-11-8_-11-7insC
ENST00000256078.10:c.-11-8_-11-7insC MANE Plus Clinical	ENSP00000256078.5:n.-11-8_-11-7insC
ENST00000311936.8:c.-11-8_-11-7insC MANE Select	ENSP00000308495.3:n.-11-8_-11-7insC
ENST00000256078.8:c.-11-8_-11-7insC	ENSP00000256078.4:n.-11-8_-11-7insC
ENST00000311936.7:c.-11-8_-11-7insC	ENSP00000308495.3:n.-11-8_-11-7insC
ENST00000556131.1:c.-11-8_-11-7insC	ENSP00000451856.1:n.-11-8_-11-7insC
ENST00000557334.5:c.-11-8_-11-7insC	ENSP00000452512.1:n.-11-8_-11-7insC
NM_004985.4:c.-11-8_-11-7insC	NP_004976.2:n.-11-8_-11-7insC
NM_033360.3:c.-11-8_-11-7insC	NP_203524.1:n.-11-8_-11-7insC
XM_006719069.2:c.-11-8_-11-7insC	XP_006719132.1:n.-11-8_-11-7insC
XM_011520653.1:c.-11-8_-11-7insC	XP_011518955.1:n.-11-8_-11-7insC
XM_006719069.4:c.-11-8_-11-7insC	XP_006719132.1:n.-11-8_-11-7insC
XM_011520653.3:c.-11-8_-11-7insC	XP_011518955.1:n.-11-8_-11-7insC
NM_001369786.1:c.-11-8_-11-7insC	NP_001356715.1:n.-11-8_-11-7insC
NM_001369787.1:c.-11-8_-11-7insC	NP_001356716.1:n.-11-8_-11-7insC
NM_004985.5:c.-11-8_-11-7insC MANE Select	NP_004976.2:n.-11-8_-11-7insC
NM_033360.4:c.-11-8_-11-7insC MANE Plus Clinical	NP_203524.1:n.-11-8_-11-7insC