Canonical Allele Identifier: CA891842143

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25245350_25245360delinsTCAGCTCCAAA , CM000674.2:g.25245350_25245360delinsTCAGCTCCAAA	GRCh38
NC_000012.11:g.25398284_25398294delinsTCAGCTCCAAA , CM000674.1:g.25398284_25398294delinsTCAGCTCCAAA	GRCh37
NC_000012.10:g.25289551_25289561delinsTCAGCTCCAAA	NCBI36
NG_007524.1:g.10561_10571delinsTTTGGAGCTGA
NG_007524.2:g.10644_10654delinsTTTGGAGCTGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000556131.2:c.25_35delinsTTTGGAGCTGA	ENSP00000451856.1:p.Val9_Gly12delinsPheGl...
ENST00000557334.6:c.25_35delinsTTTGGAGCTGA	ENSP00000452512.1:p.Val9_Gly12delinsPheGl...
ENST00000685328.1:c.25_35delinsTTTGGAGCTGA	ENSP00000508921.1:p.Val9_Gly12delinsPheGl...
ENST00000686877.1:c.25_35delinsTTTGGAGCTGA	ENSP00000510431.1:p.Val9_Gly12delinsPheGl...
ENST00000686969.1:c.25_35delinsTTTGGAGCTGA	ENSP00000510479.1:p.Val9_Gly12delinsPheGl...
ENST00000687356.1:c.25_35delinsTTTGGAGCTGA	ENSP00000510511.1:p.Val9_Gly12delinsPheGl...
ENST00000688940.1:c.25_35delinsTTTGGAGCTGA	ENSP00000509238.1:p.Val9_Gly12delinsPheGl...
ENST00000690804.1:c.25_35delinsTTTGGAGCTGA	ENSP00000508568.1:p.Val9_Gly12delinsPheGl...
ENST00000692768.1:c.-88+5391_-88+5401delinsTTTGGAGCTGA	ENSP00000510254.1:n.-88+5391_-88+5401deli...
ENST00000693229.1:c.25_35delinsTTTGGAGCTGA	ENSP00000509223.1:p.Val9_Gly12delinsPheGl...
ENST00000256078.10:c.25_35delinsTTTGGAGCTGA MANE Plus Clinical	ENSP00000256078.5:p.Val9_Gly12delinsPheGl...
ENST00000311936.8:c.25_35delinsTTTGGAGCTGA MANE Select	ENSP00000308495.3:p.Val9_Gly12delinsPheGl...
ENST00000256078.8:c.25_35delinsTTTGGAGCTGA	ENSP00000256078.4:p.Val9_Gly12delinsPheGl...
ENST00000311936.7:c.25_35delinsTTTGGAGCTGA	ENSP00000308495.3:p.Val9_Gly12delinsPheGl...
ENST00000556131.1:c.25_35delinsTTTGGAGCTGA	ENSP00000451856.1:p.Val9_Gly12delinsPheGl...
ENST00000557334.5:c.25_35delinsTTTGGAGCTGA	ENSP00000452512.1:p.Val9_Gly12delinsPheGl...
NM_004985.4:c.25_35delinsTTTGGAGCTGA	NP_004976.2:p.Val9_Gly12delinsPheGlyAlaAs...
NM_033360.3:c.25_35delinsTTTGGAGCTGA	NP_203524.1:p.Val9_Gly12delinsPheGlyAlaAs...
XM_006719069.2:c.25_35delinsTTTGGAGCTGA	XP_006719132.1:p.Val9_Gly12delinsPheGlyAl...
XM_011520653.1:c.25_35delinsTTTGGAGCTGA	XP_011518955.1:p.Val9_Gly12delinsPheGlyAl...
XM_006719069.4:c.25_35delinsTTTGGAGCTGA	XP_006719132.1:p.Val9_Gly12delinsPheGlyAl...
XM_011520653.3:c.25_35delinsTTTGGAGCTGA	XP_011518955.1:p.Val9_Gly12delinsPheGlyAl...
NM_001369786.1:c.25_35delinsTTTGGAGCTGA	NP_001356715.1:p.Val9_Gly12delinsPheGlyAl...
NM_001369787.1:c.25_35delinsTTTGGAGCTGA	NP_001356716.1:p.Val9_Gly12delinsPheGlyAl...
NM_004985.5:c.25_35delinsTTTGGAGCTGA MANE Select	NP_004976.2:p.Val9_Gly12delinsPheGlyAlaAs...
NM_033360.4:c.25_35delinsTTTGGAGCTGA MANE Plus Clinical	NP_203524.1:p.Val9_Gly12delinsPheGlyAlaAs...