Canonical Allele Identifier: CA2794888711

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209763_25209764dup , CM000674.2:g.25209763_25209764dup	GRCh38
NC_000012.11:g.25362697_25362698dup , CM000674.1:g.25362697_25362698dup	GRCh37
NC_000012.10:g.25253964_25253965dup	NCBI36
NG_007524.1:g.46157_46158dup
NG_007524.2:g.46240_46241dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*31_*32dup	ENSP00000452512.1:n.*31_*32dup
ENST00000685328.1:c.*31_*32dup	ENSP00000508921.1:n.*31_*32dup
ENST00000686877.1:c.*569_*570dup	ENSP00000510431.1:n.*569_*570dup
ENST00000687356.1:c.*296_*297dup	ENSP00000510511.1:n.*296_*297dup
ENST00000688228.1:n.1072_1073dup
ENST00000688940.1:c.*31_*32dup	ENSP00000509238.1:n.*31_*32dup
ENST00000690406.1:c.401_402dup
ENST00000690804.1:c.*559_*560dup	ENSP00000508568.1:n.*559_*560dup
ENST00000692768.1:c.*31_*32dup	ENSP00000510254.1:n.*31_*32dup
ENST00000693229.1:c.*31_*32dup	ENSP00000509223.1:n.*31_*32dup
ENST00000256078.10:c.*152_*153dup MANE Plus Clinical	ENSP00000256078.5:n.*152_*153dup
ENST00000311936.8:c.*31_*32dup MANE Select	ENSP00000308495.3:n.*31_*32dup
ENST00000256078.8:c.*152_*153dup	ENSP00000256078.4:n.*152_*153dup
ENST00000311936.7:c.*31_*32dup	ENSP00000308495.3:n.*31_*32dup
ENST00000557334.5:c.*31_*32dup	ENSP00000452512.1:n.*31_*32dup
NM_004985.4:c.*31_*32dup	NP_004976.2:n.*31_*32dup
NM_033360.3:c.*152_*153dup	NP_203524.1:n.*152_*153dup
XM_011520653.1:c.*31_*32dup	XP_011518955.1:n.*31_*32dup
XM_011520653.3:c.*31_*32dup	XP_011518955.1:n.*31_*32dup
NM_001369786.1:c.*152_*153dup	NP_001356715.1:n.*152_*153dup
NM_001369787.1:c.*31_*32dup	NP_001356716.1:n.*31_*32dup
NM_004985.5:c.*31_*32dup MANE Select	NP_004976.2:n.*31_*32dup
NM_033360.4:c.*152_*153dup MANE Plus Clinical	NP_203524.1:n.*152_*153dup