Canonical Allele Identifier: CA654638409

Gene: KRAS

Linked Data

• COSMIC: COSN18781774

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225287_25225288insTTTT , CM000674.2:g.25225287_25225288insTTTT	GRCh38
NC_000012.11:g.25378221_25378222insTTTT , CM000674.1:g.25378221_25378222insTTTT	GRCh37
NC_000012.10:g.25269488_25269489insTTTT	NCBI36
NG_007524.1:g.30636_30637insAAAA
NG_007524.2:g.30719_30720insAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15374_112-15373insAAAA	ENSP00000452512.1:n.112-15374_112-15373insAAAA
ENST00000685328.1:c.450+329_450+330insAAAA	ENSP00000508921.1:n.450+329_450+330insAAAA
ENST00000686877.1:c.*421+329_*421+330insAAAA	ENSP00000510431.1:n.*421+329_*421+330insAAAA
ENST00000687356.1:c.*148+329_*148+330insAAAA	ENSP00000510511.1:n.*148+329_*148+330insAAAA
ENST00000688228.1:n.924+329_924+330insAAAA
ENST00000688940.1:c.450+329_450+330insAAAA	ENSP00000509238.1:n.450+329_450+330insAAAA
ENST00000690406.1:c.160+329_160+330insAAAA
ENST00000690804.1:c.*411+329_*411+330insAAAA	ENSP00000508568.1:n.*411+329_*411+330insAAAA
ENST00000692768.1:c.252+329_252+330insAAAA	ENSP00000510254.1:n.252+329_252+330insAAAA
ENST00000693229.1:c.375+329_375+330insAAAA	ENSP00000509223.1:n.375+329_375+330insAAAA
ENST00000256078.10:c.450+329_450+330insAAAA MANE Plus Clinical	ENSP00000256078.5:n.450+329_450+330insAAAA
ENST00000311936.8:c.450+329_450+330insAAAA MANE Select	ENSP00000308495.3:n.450+329_450+330insAAAA
ENST00000256078.8:c.450+329_450+330insAAAA	ENSP00000256078.4:n.450+329_450+330insAAAA
ENST00000311936.7:c.450+329_450+330insAAAA	ENSP00000308495.3:n.450+329_450+330insAAAA
ENST00000557334.5:c.112-15374_112-15373insAAAA	ENSP00000452512.1:n.112-15374_112-15373insAAAA
NM_004985.4:c.450+329_450+330insAAAA	NP_004976.2:n.450+329_450+330insAAAA
NM_033360.3:c.450+329_450+330insAAAA	NP_203524.1:n.450+329_450+330insAAAA
XM_006719069.2:c.450+329_450+330insAAAA	XP_006719132.1:n.450+329_450+330insAAAA
XM_011520653.1:c.450+329_450+330insAAAA	XP_011518955.1:n.450+329_450+330insAAAA
XM_006719069.4:c.450+329_450+330insAAAA	XP_006719132.1:n.450+329_450+330insAAAA
XM_011520653.3:c.450+329_450+330insAAAA	XP_011518955.1:n.450+329_450+330insAAAA
NM_001369786.1:c.450+329_450+330insAAAA	NP_001356715.1:n.450+329_450+330insAAAA
NM_001369787.1:c.450+329_450+330insAAAA	NP_001356716.1:n.450+329_450+330insAAAA
NM_004985.5:c.450+329_450+330insAAAA MANE Select	NP_004976.2:n.450+329_450+330insAAAA
NM_033360.4:c.450+329_450+330insAAAA MANE Plus Clinical	NP_203524.1:n.450+329_450+330insAAAA