Canonical Allele Identifier: CA2580085326

Gene: KRAS

Linked Data

• ClinVar Variation Id: 1710998
• ClinVar RCV Id: RCV002292285

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25245275_25245276insG , CM000674.2:g.25245275_25245276insG	GRCh38
NC_000012.11:g.25398209_25398210insG , CM000674.1:g.25398209_25398210insG	GRCh37
NC_000012.10:g.25289476_25289477insG	NCBI36
NG_007524.1:g.10645_10646insC
NG_007524.2:g.10728_10729insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000556131.2:c.109_110insC	ENSP00000451856.1:p.Glu37AlafsTer15
ENST00000557334.6:c.109_110insC	ENSP00000452512.1:p.Glu37AlafsTer4
ENST00000685328.1:c.109_110insC	ENSP00000508921.1:p.Glu37AlafsTer11
ENST00000686877.1:c.109_110insC	ENSP00000510431.1:p.Glu37AlafsTer?
ENST00000686969.1:c.109_110insC	ENSP00000510479.1:p.Glu37AlafsTer15
ENST00000687356.1:c.109_110insC	ENSP00000510511.1:p.Glu37AlafsTer18
ENST00000688940.1:c.109_110insC	ENSP00000509238.1:p.Glu37AlafsTer11
ENST00000690804.1:c.109_110insC	ENSP00000508568.1:p.Glu37AlafsTer19
ENST00000692768.1:c.-88+5475_-88+5476insC	ENSP00000510254.1:n.-88+5475_-88+5476insC
ENST00000693229.1:c.109_110insC	ENSP00000509223.1:p.Glu37AlafsTer25
ENST00000256078.10:c.109_110insC MANE Plus Clinical	ENSP00000256078.5:p.Glu37AlafsTer11
ENST00000311936.8:c.109_110insC MANE Select	ENSP00000308495.3:p.Glu37AlafsTer11
ENST00000256078.8:c.109_110insC	ENSP00000256078.4:p.Glu37AlafsTer11
ENST00000311936.7:c.109_110insC	ENSP00000308495.3:p.Glu37AlafsTer11
ENST00000556131.1:c.109_110insC	ENSP00000451856.1:p.Glu37AlafsTer15
ENST00000557334.5:c.109_110insC	ENSP00000452512.1:p.Glu37AlafsTer4
NM_004985.4:c.109_110insC	NP_004976.2:p.Glu37AlafsTer11
NM_033360.3:c.109_110insC	NP_203524.1:p.Glu37AlafsTer11
XM_006719069.2:c.109_110insC	XP_006719132.1:p.Glu37AlafsTer11
XM_011520653.1:c.109_110insC	XP_011518955.1:p.Glu37AlafsTer11
XM_006719069.4:c.109_110insC	XP_006719132.1:p.Glu37AlafsTer11
XM_011520653.3:c.109_110insC	XP_011518955.1:p.Glu37AlafsTer11
NM_001369786.1:c.109_110insC	NP_001356715.1:p.Glu37AlafsTer11
NM_001369787.1:c.109_110insC	NP_001356716.1:p.Glu37AlafsTer11
NM_004985.5:c.109_110insC MANE Select	NP_004976.2:p.Glu37AlafsTer11
NM_033360.4:c.109_110insC MANE Plus Clinical	NP_203524.1:p.Glu37AlafsTer11