Canonical Allele Identifier: CA2022885005

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25210184_25210187delinsCAGG , CM000674.2:g.25210184_25210187delinsCAGG	GRCh38
NC_000012.11:g.25363118_25363121delinsCAGG , CM000674.1:g.25363118_25363121delinsCAGG	GRCh37
NC_000012.10:g.25254385_25254388delinsCAGG	NCBI36
NG_007524.1:g.45734_45737delinsCCTG
NG_007524.2:g.45817_45820delinsCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-276_112-273delinsCCTG	ENSP00000452512.1:n.112-276_112-273delinsCCTG
ENST00000685328.1:c.451-276_451-273delinsCCTG	ENSP00000508921.1:n.451-276_451-273delinsCCTG
ENST00000686877.1:c.*422-276_*422-273delinsCCTG	ENSP00000510431.1:n.*422-276_*422-273delinsCCTG
ENST00000687356.1:c.*149-276_*149-273delinsCCTG	ENSP00000510511.1:n.*149-276_*149-273delinsCCTG
ENST00000688228.1:n.925-276_925-273delinsCCTG
ENST00000688940.1:c.451-276_451-273delinsCCTG	ENSP00000509238.1:n.451-276_451-273delinsCCTG
ENST00000690406.1:c.254-276_254-273delinsCCTG
ENST00000690804.1:c.*412-276_*412-273delinsCCTG	ENSP00000508568.1:n.*412-276_*412-273delinsCCTG
ENST00000692768.1:c.253-276_253-273delinsCCTG	ENSP00000510254.1:n.253-276_253-273delinsCCTG
ENST00000693229.1:c.376-276_376-273delinsCCTG	ENSP00000509223.1:n.376-276_376-273delinsCCTG
ENST00000256078.10:c.*5-276_*5-273delinsCCTG MANE Plus Clinical	ENSP00000256078.5:n.*5-276_*5-273delinsCCTG
ENST00000311936.8:c.451-276_451-273delinsCCTG MANE Select	ENSP00000308495.3:n.451-276_451-273delinsCCTG
ENST00000256078.8:c.*5-276_*5-273delinsCCTG	ENSP00000256078.4:n.*5-276_*5-273delinsCCTG
ENST00000311936.7:c.451-276_451-273delinsCCTG	ENSP00000308495.3:n.451-276_451-273delinsCCTG
ENST00000557334.5:c.112-276_112-273delinsCCTG	ENSP00000452512.1:n.112-276_112-273delinsCCTG
NM_004985.4:c.451-276_451-273delinsCCTG	NP_004976.2:n.451-276_451-273delinsCCTG
NM_033360.3:c.*5-276_*5-273delinsCCTG	NP_203524.1:n.*5-276_*5-273delinsCCTG
XM_006719069.2:c.*5-276_*5-273delinsCCTG	XP_006719132.1:n.*5-276_*5-273delinsCCTG
XM_011520653.1:c.451-276_451-273delinsCCTG	XP_011518955.1:n.451-276_451-273delinsCCTG
XM_006719069.4:c.*5-276_*5-273delinsCCTG	XP_006719132.1:n.*5-276_*5-273delinsCCTG
XM_011520653.3:c.451-276_451-273delinsCCTG	XP_011518955.1:n.451-276_451-273delinsCCTG
NM_001369786.1:c.*5-276_*5-273delinsCCTG	NP_001356715.1:n.*5-276_*5-273delinsCCTG
NM_001369787.1:c.451-276_451-273delinsCCTG	NP_001356716.1:n.451-276_451-273delinsCCTG
NM_004985.5:c.451-276_451-273delinsCCTG MANE Select	NP_004976.2:n.451-276_451-273delinsCCTG
NM_033360.4:c.*5-276_*5-273delinsCCTG MANE Plus Clinical	NP_203524.1:n.*5-276_*5-273delinsCCTG