Canonical Allele Identifier: CA2022884990

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25210164_25210168delinsATAAG , CM000674.2:g.25210164_25210168delinsATAAG	GRCh38
NC_000012.11:g.25363098_25363102delinsATAAG , CM000674.1:g.25363098_25363102delinsATAAG	GRCh37
NC_000012.10:g.25254365_25254369delinsATAAG	NCBI36
NG_007524.1:g.45753_45757delinsCTTAT
NG_007524.2:g.45836_45840delinsCTTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-257_112-253delinsCTTAT	ENSP00000452512.1:n.112-257_112-253delinsCTTAT
ENST00000685328.1:c.451-257_451-253delinsCTTAT	ENSP00000508921.1:n.451-257_451-253delinsCTTAT
ENST00000686877.1:c.*422-257_*422-253delinsCTTAT	ENSP00000510431.1:n.*422-257_*422-253delinsCTTAT
ENST00000687356.1:c.*149-257_*149-253delinsCTTAT	ENSP00000510511.1:n.*149-257_*149-253delinsCTTAT
ENST00000688228.1:n.925-257_925-253delinsCTTAT
ENST00000688940.1:c.451-257_451-253delinsCTTAT	ENSP00000509238.1:n.451-257_451-253delinsCTTAT
ENST00000690406.1:c.254-257_254-253delinsCTTAT
ENST00000690804.1:c.*412-257_*412-253delinsCTTAT	ENSP00000508568.1:n.*412-257_*412-253delinsCTTAT
ENST00000692768.1:c.253-257_253-253delinsCTTAT	ENSP00000510254.1:n.253-257_253-253delinsCTTAT
ENST00000693229.1:c.376-257_376-253delinsCTTAT	ENSP00000509223.1:n.376-257_376-253delinsCTTAT
ENST00000256078.10:c.*5-257_*5-253delinsCTTAT MANE Plus Clinical	ENSP00000256078.5:n.*5-257_*5-253delinsCTTAT
ENST00000311936.8:c.451-257_451-253delinsCTTAT MANE Select	ENSP00000308495.3:n.451-257_451-253delinsCTTAT
ENST00000256078.8:c.*5-257_*5-253delinsCTTAT	ENSP00000256078.4:n.*5-257_*5-253delinsCTTAT
ENST00000311936.7:c.451-257_451-253delinsCTTAT	ENSP00000308495.3:n.451-257_451-253delinsCTTAT
ENST00000557334.5:c.112-257_112-253delinsCTTAT	ENSP00000452512.1:n.112-257_112-253delinsCTTAT
NM_004985.4:c.451-257_451-253delinsCTTAT	NP_004976.2:n.451-257_451-253delinsCTTAT
NM_033360.3:c.*5-257_*5-253delinsCTTAT	NP_203524.1:n.*5-257_*5-253delinsCTTAT
XM_006719069.2:c.*5-257_*5-253delinsCTTAT	XP_006719132.1:n.*5-257_*5-253delinsCTTAT
XM_011520653.1:c.451-257_451-253delinsCTTAT	XP_011518955.1:n.451-257_451-253delinsCTTAT
XM_006719069.4:c.*5-257_*5-253delinsCTTAT	XP_006719132.1:n.*5-257_*5-253delinsCTTAT
XM_011520653.3:c.451-257_451-253delinsCTTAT	XP_011518955.1:n.451-257_451-253delinsCTTAT
NM_001369786.1:c.*5-257_*5-253delinsCTTAT	NP_001356715.1:n.*5-257_*5-253delinsCTTAT
NM_001369787.1:c.451-257_451-253delinsCTTAT	NP_001356716.1:n.451-257_451-253delinsCTTAT
NM_004985.5:c.451-257_451-253delinsCTTAT MANE Select	NP_004976.2:n.451-257_451-253delinsCTTAT
NM_033360.4:c.*5-257_*5-253delinsCTTAT MANE Plus Clinical	NP_203524.1:n.*5-257_*5-253delinsCTTAT