Canonical Allele Identifier: CA2022884634

Gene: KRAS

Linked Data

• dbSNP Id: rs1951184231

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209865dup , CM000674.2:g.25209865dup	GRCh38
NC_000012.11:g.25362799dup , CM000674.1:g.25362799dup	GRCh37
NC_000012.10:g.25254066dup	NCBI36
NG_007524.1:g.46056dup
NG_007524.2:g.46139dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.158dup	ENSP00000452512.1:p.His53GlnfsTer2
ENST00000685328.1:c.497dup	ENSP00000508921.1:p.His166GlnfsTer2
ENST00000686877.1:c.*468dup	ENSP00000510431.1:n.*468dup
ENST00000687356.1:c.*195dup	ENSP00000510511.1:n.*195dup
ENST00000688228.1:n.971dup
ENST00000688940.1:c.497dup	ENSP00000509238.1:p.His166GlnfsTer2
ENST00000690406.1:c.300dup
ENST00000690804.1:c.*458dup	ENSP00000508568.1:n.*458dup
ENST00000692768.1:c.299dup	ENSP00000510254.1:p.His100GlnfsTer2
ENST00000693229.1:c.422dup	ENSP00000509223.1:p.His141GlnfsTer2
ENST00000256078.10:c.*51dup MANE Plus Clinical	ENSP00000256078.5:n.*51dup
ENST00000311936.8:c.497dup MANE Select	ENSP00000308495.3:p.His166GlnfsTer2
ENST00000256078.8:c.*51dup	ENSP00000256078.4:n.*51dup
ENST00000311936.7:c.497dup	ENSP00000308495.3:p.His166GlnfsTer2
ENST00000557334.5:c.158dup	ENSP00000452512.1:p.His53GlnfsTer2
NM_004985.4:c.497dup	NP_004976.2:p.His166GlnfsTer2
NM_033360.3:c.*51dup	NP_203524.1:n.*51dup
XM_006719069.2:c.*51dup	XP_006719132.1:n.*51dup
XM_011520653.1:c.497dup	XP_011518955.1:p.His166GlnfsTer2
XM_006719069.4:c.*51dup	XP_006719132.1:n.*51dup
XM_011520653.3:c.497dup	XP_011518955.1:p.His166GlnfsTer2
NM_001369786.1:c.*51dup	NP_001356715.1:n.*51dup
NM_001369787.1:c.497dup	NP_001356716.1:p.His166GlnfsTer2
NM_004985.5:c.497dup MANE Select	NP_004976.2:p.His166GlnfsTer2
NM_033360.4:c.*51dup MANE Plus Clinical	NP_203524.1:n.*51dup