Canonical Allele Identifier: CA2794888709

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209714_25209725del , CM000674.2:g.25209714_25209725del	GRCh38
NC_000012.11:g.25362648_25362659del , CM000674.1:g.25362648_25362659del	GRCh37
NC_000012.10:g.25253915_25253926del	NCBI36
NG_007524.1:g.46204_46215del
NG_007524.2:g.46287_46298del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*78_*89del	ENSP00000452512.1:n.*78_*89del
ENST00000685328.1:c.*78_*89del	ENSP00000508921.1:n.*78_*89del
ENST00000686877.1:c.*616_*627del	ENSP00000510431.1:n.*616_*627del
ENST00000687356.1:c.*343_*354del	ENSP00000510511.1:n.*343_*354del
ENST00000688228.1:n.1119_1130del
ENST00000688940.1:c.*78_*89del	ENSP00000509238.1:n.*78_*89del
ENST00000690406.1:c.448_459del
ENST00000690804.1:c.*606_*617del	ENSP00000508568.1:n.*606_*617del
ENST00000692768.1:c.*78_*89del	ENSP00000510254.1:n.*78_*89del
ENST00000693229.1:c.*78_*89del	ENSP00000509223.1:n.*78_*89del
ENST00000256078.10:c.*199_*210del MANE Plus Clinical	ENSP00000256078.5:n.*199_*210del
ENST00000311936.8:c.*78_*89del MANE Select	ENSP00000308495.3:n.*78_*89del
ENST00000256078.8:c.*199_*210del	ENSP00000256078.4:n.*199_*210del
ENST00000311936.7:c.*78_*89del	ENSP00000308495.3:n.*78_*89del
ENST00000557334.5:c.*78_*89del	ENSP00000452512.1:n.*78_*89del
NM_004985.4:c.*78_*89del	NP_004976.2:n.*78_*89del
NM_033360.3:c.*199_*210del	NP_203524.1:n.*199_*210del
XM_011520653.1:c.*78_*89del	XP_011518955.1:n.*78_*89del
XM_011520653.3:c.*78_*89del	XP_011518955.1:n.*78_*89del
NM_001369786.1:c.*199_*210del	NP_001356715.1:n.*199_*210del
NM_001369787.1:c.*78_*89del	NP_001356716.1:n.*78_*89del
NM_004985.5:c.*78_*89del MANE Select	NP_004976.2:n.*78_*89del
NM_033360.4:c.*199_*210del MANE Plus Clinical	NP_203524.1:n.*199_*210del