Canonical Allele Identifier: CA2022885042

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25210249_25210251delinsCAT , CM000674.2:g.25210249_25210251delinsCAT	GRCh38
NC_000012.11:g.25363183_25363185delinsCAT , CM000674.1:g.25363183_25363185delinsCAT	GRCh37
NC_000012.10:g.25254450_25254452delinsCAT	NCBI36
NG_007524.1:g.45670_45672delinsATG
NG_007524.2:g.45753_45755delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-340_112-338delinsATG	ENSP00000452512.1:n.112-340_112-338delinsATG
ENST00000685328.1:c.451-340_451-338delinsATG	ENSP00000508921.1:n.451-340_451-338delinsATG
ENST00000686877.1:c.*422-340_*422-338delinsATG	ENSP00000510431.1:n.*422-340_*422-338delinsATG
ENST00000687356.1:c.*149-340_*149-338delinsATG	ENSP00000510511.1:n.*149-340_*149-338delinsATG
ENST00000688228.1:n.925-340_925-338delinsATG
ENST00000688940.1:c.451-340_451-338delinsATG	ENSP00000509238.1:n.451-340_451-338delinsATG
ENST00000690406.1:c.254-340_254-338delinsATG
ENST00000690804.1:c.*412-340_*412-338delinsATG	ENSP00000508568.1:n.*412-340_*412-338delinsATG
ENST00000692768.1:c.253-340_253-338delinsATG	ENSP00000510254.1:n.253-340_253-338delinsATG
ENST00000693229.1:c.376-340_376-338delinsATG	ENSP00000509223.1:n.376-340_376-338delinsATG
ENST00000256078.10:c.*5-340_*5-338delinsATG MANE Plus Clinical	ENSP00000256078.5:n.*5-340_*5-338delinsATG
ENST00000311936.8:c.451-340_451-338delinsATG MANE Select	ENSP00000308495.3:n.451-340_451-338delinsATG
ENST00000256078.8:c.*5-340_*5-338delinsATG	ENSP00000256078.4:n.*5-340_*5-338delinsATG
ENST00000311936.7:c.451-340_451-338delinsATG	ENSP00000308495.3:n.451-340_451-338delinsATG
ENST00000557334.5:c.112-340_112-338delinsATG	ENSP00000452512.1:n.112-340_112-338delinsATG
NM_004985.4:c.451-340_451-338delinsATG	NP_004976.2:n.451-340_451-338delinsATG
NM_033360.3:c.*5-340_*5-338delinsATG	NP_203524.1:n.*5-340_*5-338delinsATG
XM_006719069.2:c.*5-340_*5-338delinsATG	XP_006719132.1:n.*5-340_*5-338delinsATG
XM_011520653.1:c.451-340_451-338delinsATG	XP_011518955.1:n.451-340_451-338delinsATG
XM_006719069.4:c.*5-340_*5-338delinsATG	XP_006719132.1:n.*5-340_*5-338delinsATG
XM_011520653.3:c.451-340_451-338delinsATG	XP_011518955.1:n.451-340_451-338delinsATG
NM_001369786.1:c.*5-340_*5-338delinsATG	NP_001356715.1:n.*5-340_*5-338delinsATG
NM_001369787.1:c.451-340_451-338delinsATG	NP_001356716.1:n.451-340_451-338delinsATG
NM_004985.5:c.451-340_451-338delinsATG MANE Select	NP_004976.2:n.451-340_451-338delinsATG
NM_033360.4:c.*5-340_*5-338delinsATG MANE Plus Clinical	NP_203524.1:n.*5-340_*5-338delinsATG