Canonical Allele Identifier: CA345822

Gene: KRAS

Linked Data

• ClinVar Variation Id: 155804
• ClinVar RCV Id: RCV000143908
• dbSNP Id: rs397517043
• MyVariant Identifiers: chr12:g.25362763_25362765dupTTC (hg19) ; chr12:g.25362762_25362763insTTC (hg19) ; chr12:g.25209829_25209831dupTTC (hg38) ; chr12:g.25209828_25209829insTTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209834_25209836dup , CM000674.2:g.25209834_25209836dup	GRCh38
NC_000012.11:g.25362768_25362770dup , CM000674.1:g.25362768_25362770dup	GRCh37
NC_000012.10:g.25254035_25254037dup	NCBI36
NG_007524.1:g.46090_46092dup
NG_007524.2:g.46173_46175dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.192_194dup	ENSP00000452512.1:p.Lys65_Lys66insLys
ENST00000685328.1:c.531_533dup	ENSP00000508921.1:p.Lys178_Lys179insLys
ENST00000686877.1:c.*502_*504dup	ENSP00000510431.1:n.*502_*504dup
ENST00000687356.1:c.*229_*231dup	ENSP00000510511.1:n.*229_*231dup
ENST00000688228.1:n.1005_1007dup
ENST00000688940.1:c.531_533dup	ENSP00000509238.1:p.Lys178_Lys179insLys
ENST00000690406.1:c.334_336dup
ENST00000690804.1:c.*492_*494dup	ENSP00000508568.1:n.*492_*494dup
ENST00000692768.1:c.333_335dup	ENSP00000510254.1:p.Lys112_Lys113insLys
ENST00000693229.1:c.456_458dup	ENSP00000509223.1:p.Lys153_Lys154insLys
ENST00000256078.10:c.*85_*87dup MANE Plus Clinical	ENSP00000256078.5:n.*85_*87dup
ENST00000311936.8:c.531_533dup MANE Select	ENSP00000308495.3:p.Lys178_Lys179insLys
ENST00000256078.8:c.*85_*87dup	ENSP00000256078.4:n.*85_*87dup
ENST00000311936.7:c.531_533dup	ENSP00000308495.3:p.Lys178_Lys179insLys
ENST00000557334.5:c.192_194dup	ENSP00000452512.1:p.Lys65_Lys66insLys
NM_004985.4:c.531_533dup	NP_004976.2:p.Lys178_Lys179insLys
NM_033360.3:c.*85_*87dup	NP_203524.1:n.*85_*87dup
XM_006719069.2:c.*85_*87dup	XP_006719132.1:n.*85_*87dup
XM_011520653.1:c.531_533dup	XP_011518955.1:p.Lys178_Lys179insLys
XM_006719069.4:c.*85_*87dup	XP_006719132.1:n.*85_*87dup
XM_011520653.3:c.531_533dup	XP_011518955.1:p.Lys178_Lys179insLys
NM_001369786.1:c.*85_*87dup	NP_001356715.1:n.*85_*87dup
NM_001369787.1:c.531_533dup	NP_001356716.1:p.Lys178_Lys179insLys
NM_004985.5:c.531_533dup MANE Select	NP_004976.2:p.Lys178_Lys179insLys
NM_033360.4:c.*85_*87dup MANE Plus Clinical	NP_203524.1:n.*85_*87dup