Canonical Allele Identifier: CA919045362

Gene: KRAS

Linked Data

• dbSNP Id: rs1592794345

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25210226_25210240del , CM000674.2:g.25210226_25210240del	GRCh38
NC_000012.11:g.25363160_25363174del , CM000674.1:g.25363160_25363174del	GRCh37
NC_000012.10:g.25254427_25254441del	NCBI36
NG_007524.1:g.45684_45698del
NG_007524.2:g.45767_45781del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-326_112-312del	ENSP00000452512.1:n.112-326_112-312del
ENST00000685328.1:c.451-326_451-312del	ENSP00000508921.1:n.451-326_451-312del
ENST00000686877.1:c.*422-326_*422-312del	ENSP00000510431.1:n.*422-326_*422-312del
ENST00000687356.1:c.*149-326_*149-312del	ENSP00000510511.1:n.*149-326_*149-312del
ENST00000688228.1:n.925-326_925-312del
ENST00000688940.1:c.451-326_451-312del	ENSP00000509238.1:n.451-326_451-312del
ENST00000690406.1:c.254-326_254-312del
ENST00000690804.1:c.*412-326_*412-312del	ENSP00000508568.1:n.*412-326_*412-312del
ENST00000692768.1:c.253-326_253-312del	ENSP00000510254.1:n.253-326_253-312del
ENST00000693229.1:c.376-326_376-312del	ENSP00000509223.1:n.376-326_376-312del
ENST00000256078.10:c.*5-326_*5-312del MANE Plus Clinical	ENSP00000256078.5:n.*5-326_*5-312del
ENST00000311936.8:c.451-326_451-312del MANE Select	ENSP00000308495.3:n.451-326_451-312del
ENST00000256078.8:c.*5-326_*5-312del	ENSP00000256078.4:n.*5-326_*5-312del
ENST00000311936.7:c.451-326_451-312del	ENSP00000308495.3:n.451-326_451-312del
ENST00000557334.5:c.112-326_112-312del	ENSP00000452512.1:n.112-326_112-312del
NM_004985.4:c.451-326_451-312del	NP_004976.2:n.451-326_451-312del
NM_033360.3:c.*5-326_*5-312del	NP_203524.1:n.*5-326_*5-312del
XM_006719069.2:c.*5-326_*5-312del	XP_006719132.1:n.*5-326_*5-312del
XM_011520653.1:c.451-326_451-312del	XP_011518955.1:n.451-326_451-312del
XM_006719069.4:c.*5-326_*5-312del	XP_006719132.1:n.*5-326_*5-312del
XM_011520653.3:c.451-326_451-312del	XP_011518955.1:n.451-326_451-312del
NM_001369786.1:c.*5-326_*5-312del	NP_001356715.1:n.*5-326_*5-312del
NM_001369787.1:c.451-326_451-312del	NP_001356716.1:n.451-326_451-312del
NM_004985.5:c.451-326_451-312del MANE Select	NP_004976.2:n.451-326_451-312del
NM_033360.4:c.*5-326_*5-312del MANE Plus Clinical	NP_203524.1:n.*5-326_*5-312del