Canonical Allele Identifier: CA2022897862

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25245153_25245158delinsATAACT , CM000674.2:g.25245153_25245158delinsATAACT	GRCh38
NC_000012.11:g.25398087_25398092delinsATAACT , CM000674.1:g.25398087_25398092delinsATAACT	GRCh37
NC_000012.10:g.25289354_25289359delinsATAACT	NCBI36
NG_007524.1:g.10763_10768delinsAGTTAT
NG_007524.2:g.10846_10851delinsAGTTAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000556131.2:c.111+116_111+121delinsAGTTAT	ENSP00000451856.1:n.111+116_111+121delins...
ENST00000557334.6:c.111+116_111+121delinsAGTTAT	ENSP00000452512.1:n.111+116_111+121delins...
ENST00000685328.1:c.111+116_111+121delinsAGTTAT	ENSP00000508921.1:n.111+116_111+121delins...
ENST00000686877.1:c.111+116_111+121delinsAGTTAT	ENSP00000510431.1:n.111+116_111+121delins...
ENST00000686969.1:c.111+116_111+121delinsAGTTAT	ENSP00000510479.1:n.111+116_111+121delins...
ENST00000687356.1:c.111+116_111+121delinsAGTTAT	ENSP00000510511.1:n.111+116_111+121delins...
ENST00000688940.1:c.111+116_111+121delinsAGTTAT	ENSP00000509238.1:n.111+116_111+121delins...
ENST00000690804.1:c.111+116_111+121delinsAGTTAT	ENSP00000508568.1:n.111+116_111+121delins...
ENST00000692768.1:c.-88+5593_-88+5598delinsAGTTAT	ENSP00000510254.1:n.-88+5593_-88+5598deli...
ENST00000693229.1:c.111+116_111+121delinsAGTTAT	ENSP00000509223.1:n.111+116_111+121delins...
ENST00000256078.10:c.111+116_111+121delinsAGTTAT MANE Plus Clinical	ENSP00000256078.5:n.111+116_111+121delins...
ENST00000311936.8:c.111+116_111+121delinsAGTTAT MANE Select	ENSP00000308495.3:n.111+116_111+121delins...
ENST00000256078.8:c.111+116_111+121delinsAGTTAT	ENSP00000256078.4:n.111+116_111+121delins...
ENST00000311936.7:c.111+116_111+121delinsAGTTAT	ENSP00000308495.3:n.111+116_111+121delins...
ENST00000556131.1:c.111+116_111+121delinsAGTTAT	ENSP00000451856.1:n.111+116_111+121delins...
ENST00000557334.5:c.111+116_111+121delinsAGTTAT	ENSP00000452512.1:n.111+116_111+121delins...
NM_004985.4:c.111+116_111+121delinsAGTTAT	NP_004976.2:n.111+116_111+121delinsAGTTAT...
NM_033360.3:c.111+116_111+121delinsAGTTAT	NP_203524.1:n.111+116_111+121delinsAGTTAT...
XM_006719069.2:c.111+116_111+121delinsAGTTAT	XP_006719132.1:n.111+116_111+121delinsAGT...
XM_011520653.1:c.111+116_111+121delinsAGTTAT	XP_011518955.1:n.111+116_111+121delinsAGT...
XM_006719069.4:c.111+116_111+121delinsAGTTAT	XP_006719132.1:n.111+116_111+121delinsAGT...
XM_011520653.3:c.111+116_111+121delinsAGTTAT	XP_011518955.1:n.111+116_111+121delinsAGT...
NM_001369786.1:c.111+116_111+121delinsAGTTAT	NP_001356715.1:n.111+116_111+121delinsAGT...
NM_001369787.1:c.111+116_111+121delinsAGTTAT	NP_001356716.1:n.111+116_111+121delinsAGT...
NM_004985.5:c.111+116_111+121delinsAGTTAT MANE Select	NP_004976.2:n.111+116_111+121delinsAGTTAT...
NM_033360.4:c.111+116_111+121delinsAGTTAT MANE Plus Clinical	NP_203524.1:n.111+116_111+121delinsAGTTAT...