Canonical Allele Identifier: CA2022884424

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209720_25209721delinsTG , CM000674.2:g.25209720_25209721delinsTG	GRCh38
NC_000012.11:g.25362654_25362655delinsTG , CM000674.1:g.25362654_25362655delinsTG	GRCh37
NC_000012.10:g.25253921_25253922delinsTG	NCBI36
NG_007524.1:g.46200_46201delinsCA
NG_007524.2:g.46283_46284delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.*74_*75delinsCA	ENSP00000452512.1:n.*74_*75delinsCA
ENST00000685328.1:c.*74_*75delinsCA	ENSP00000508921.1:n.*74_*75delinsCA
ENST00000686877.1:c.*612_*613delinsCA	ENSP00000510431.1:n.*612_*613delinsCA
ENST00000687356.1:c.*339_*340delinsCA	ENSP00000510511.1:n.*339_*340delinsCA
ENST00000688228.1:n.1115_1116delinsCA
ENST00000688940.1:c.*74_*75delinsCA	ENSP00000509238.1:n.*74_*75delinsCA
ENST00000690406.1:c.444_445delinsCA
ENST00000690804.1:c.*602_*603delinsCA	ENSP00000508568.1:n.*602_*603delinsCA
ENST00000692768.1:c.*74_*75delinsCA	ENSP00000510254.1:n.*74_*75delinsCA
ENST00000693229.1:c.*74_*75delinsCA	ENSP00000509223.1:n.*74_*75delinsCA
ENST00000256078.10:c.*195_*196delinsCA MANE Plus Clinical	ENSP00000256078.5:n.*195_*196delinsCA
ENST00000311936.8:c.*74_*75delinsCA MANE Select	ENSP00000308495.3:n.*74_*75delinsCA
ENST00000256078.8:c.*195_*196delinsCA	ENSP00000256078.4:n.*195_*196delinsCA
ENST00000311936.7:c.*74_*75delinsCA	ENSP00000308495.3:n.*74_*75delinsCA
ENST00000557334.5:c.*74_*75delinsCA	ENSP00000452512.1:n.*74_*75delinsCA
NM_004985.4:c.*74_*75delinsCA	NP_004976.2:n.*74_*75delinsCA
NM_033360.3:c.*195_*196delinsCA	NP_203524.1:n.*195_*196delinsCA
XM_011520653.1:c.*74_*75delinsCA	XP_011518955.1:n.*74_*75delinsCA
XM_011520653.3:c.*74_*75delinsCA	XP_011518955.1:n.*74_*75delinsCA
NM_001369786.1:c.*195_*196delinsCA	NP_001356715.1:n.*195_*196delinsCA
NM_001369787.1:c.*74_*75delinsCA	NP_001356716.1:n.*74_*75delinsCA
NM_004985.5:c.*74_*75delinsCA MANE Select	NP_004976.2:n.*74_*75delinsCA
NM_033360.4:c.*195_*196delinsCA MANE Plus Clinical	NP_203524.1:n.*195_*196delinsCA