Canonical Allele Identifier: CA2539001100

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209766_25209769del , CM000674.2:g.25209766_25209769del	GRCh38
NC_000012.11:g.25362700_25362703del , CM000674.1:g.25362700_25362703del	GRCh37
NC_000012.10:g.25253967_25253970del	NCBI36
NG_007524.1:g.46152_46155del
NG_007524.2:g.46235_46238del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*26_*29del	ENSP00000452512.1:n.*26_*29del
ENST00000685328.1:c.*26_*29del	ENSP00000508921.1:n.*26_*29del
ENST00000686877.1:c.*564_*567del	ENSP00000510431.1:n.*564_*567del
ENST00000687356.1:c.*291_*294del	ENSP00000510511.1:n.*291_*294del
ENST00000688228.1:n.1067_1070del
ENST00000688940.1:c.*26_*29del	ENSP00000509238.1:n.*26_*29del
ENST00000690406.1:c.396_399del
ENST00000690804.1:c.*554_*557del	ENSP00000508568.1:n.*554_*557del
ENST00000692768.1:c.*26_*29del	ENSP00000510254.1:n.*26_*29del
ENST00000693229.1:c.*26_*29del	ENSP00000509223.1:n.*26_*29del
ENST00000256078.10:c.*147_*150del MANE Plus Clinical	ENSP00000256078.5:n.*147_*150del
ENST00000311936.8:c.*26_*29del MANE Select	ENSP00000308495.3:n.*26_*29del
ENST00000256078.8:c.*147_*150del	ENSP00000256078.4:n.*147_*150del
ENST00000311936.7:c.*26_*29del	ENSP00000308495.3:n.*26_*29del
ENST00000557334.5:c.*26_*29del	ENSP00000452512.1:n.*26_*29del
NM_004985.4:c.*26_*29del	NP_004976.2:n.*26_*29del
NM_033360.3:c.*147_*150del	NP_203524.1:n.*147_*150del
XM_011520653.1:c.*26_*29del	XP_011518955.1:n.*26_*29del
XM_011520653.3:c.*26_*29del	XP_011518955.1:n.*26_*29del
NM_001369786.1:c.*147_*150del	NP_001356715.1:n.*147_*150del
NM_001369787.1:c.*26_*29del	NP_001356716.1:n.*26_*29del
NM_004985.5:c.*26_*29del MANE Select	NP_004976.2:n.*26_*29del
NM_033360.4:c.*147_*150del MANE Plus Clinical	NP_203524.1:n.*147_*150del