Canonical Allele Identifier: CA2726035151

Gene: KRAS

Linked Data

• dbSNP Id: rs2141504699

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225304_25225328del , CM000674.2:g.25225304_25225328del	GRCh38
NC_000012.11:g.25378238_25378262del , CM000674.1:g.25378238_25378262del	GRCh37
NC_000012.10:g.25269505_25269529del	NCBI36
NG_007524.1:g.30593_30617del
NG_007524.2:g.30676_30700del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15417_112-15393del	ENSP00000452512.1:n.112-15417_112-15393del
ENST00000685328.1:c.450+286_450+310del	ENSP00000508921.1:n.450+286_450+310del
ENST00000686877.1:c.*421+286_*421+310del	ENSP00000510431.1:n.*421+286_*421+310del
ENST00000687356.1:c.*148+286_*148+310del	ENSP00000510511.1:n.*148+286_*148+310del
ENST00000688228.1:n.924+286_924+310del
ENST00000688940.1:c.450+286_450+310del	ENSP00000509238.1:n.450+286_450+310del
ENST00000690406.1:c.160+286_160+310del
ENST00000690804.1:c.*411+286_*411+310del	ENSP00000508568.1:n.*411+286_*411+310del
ENST00000692768.1:c.252+286_252+310del	ENSP00000510254.1:n.252+286_252+310del
ENST00000693229.1:c.375+286_375+310del	ENSP00000509223.1:n.375+286_375+310del
ENST00000256078.10:c.450+286_450+310del MANE Plus Clinical	ENSP00000256078.5:n.450+286_450+310del
ENST00000311936.8:c.450+286_450+310del MANE Select	ENSP00000308495.3:n.450+286_450+310del
ENST00000256078.8:c.450+286_450+310del	ENSP00000256078.4:n.450+286_450+310del
ENST00000311936.7:c.450+286_450+310del	ENSP00000308495.3:n.450+286_450+310del
ENST00000557334.5:c.112-15417_112-15393del	ENSP00000452512.1:n.112-15417_112-15393del
NM_004985.4:c.450+286_450+310del	NP_004976.2:n.450+286_450+310del
NM_033360.3:c.450+286_450+310del	NP_203524.1:n.450+286_450+310del
XM_006719069.2:c.450+286_450+310del	XP_006719132.1:n.450+286_450+310del
XM_011520653.1:c.450+286_450+310del	XP_011518955.1:n.450+286_450+310del
XM_006719069.4:c.450+286_450+310del	XP_006719132.1:n.450+286_450+310del
XM_011520653.3:c.450+286_450+310del	XP_011518955.1:n.450+286_450+310del
NM_001369786.1:c.450+286_450+310del	NP_001356715.1:n.450+286_450+310del
NM_001369787.1:c.450+286_450+310del	NP_001356716.1:n.450+286_450+310del
NM_004985.5:c.450+286_450+310del MANE Select	NP_004976.2:n.450+286_450+310del
NM_033360.4:c.450+286_450+310del MANE Plus Clinical	NP_203524.1:n.450+286_450+310del