Canonical Allele Identifier: CA2022884500

Gene: KRAS

Linked Data

• dbSNP Id: rs1951183248

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209791_25209795del , CM000674.2:g.25209791_25209795del	GRCh38
NC_000012.11:g.25362725_25362729del , CM000674.1:g.25362725_25362729del	GRCh37
NC_000012.10:g.25253992_25253996del	NCBI36
NG_007524.1:g.46129_46133del
NG_007524.2:g.46212_46216del

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.*3_*7del	ENSP00000452512.1:n.*3_*7del
ENST00000685328.1:c.*3_*7del	ENSP00000508921.1:n.*3_*7del
ENST00000686877.1:c.*541_*545del	ENSP00000510431.1:n.*541_*545del
ENST00000687356.1:c.*268_*272del	ENSP00000510511.1:n.*268_*272del
ENST00000688228.1:n.1044_1048del
ENST00000688940.1:c.*3_*7del	ENSP00000509238.1:n.*3_*7del
ENST00000690406.1:c.373_377del
ENST00000690804.1:c.*531_*535del	ENSP00000508568.1:n.*531_*535del
ENST00000692768.1:c.*3_*7del	ENSP00000510254.1:n.*3_*7del
ENST00000693229.1:c.*3_*7del	ENSP00000509223.1:n.*3_*7del
ENST00000256078.10:c.*124_*128del MANE Plus Clinical	ENSP00000256078.5:n.*124_*128del
ENST00000311936.8:c.*3_*7del MANE Select	ENSP00000308495.3:n.*3_*7del
ENST00000256078.8:c.*124_*128del	ENSP00000256078.4:n.*124_*128del
ENST00000311936.7:c.*3_*7del	ENSP00000308495.3:n.*3_*7del
ENST00000557334.5:c.*3_*7del	ENSP00000452512.1:n.*3_*7del
NM_004985.4:c.*3_*7del	NP_004976.2:n.*3_*7del
NM_033360.3:c.*124_*128del	NP_203524.1:n.*124_*128del
XM_011520653.1:c.*3_*7del	XP_011518955.1:n.*3_*7del
XM_011520653.3:c.*3_*7del	XP_011518955.1:n.*3_*7del
NM_001369786.1:c.*124_*128del	NP_001356715.1:n.*124_*128del
NM_001369787.1:c.*3_*7del	NP_001356716.1:n.*3_*7del
NM_004985.5:c.*3_*7del MANE Select	NP_004976.2:n.*3_*7del
NM_033360.4:c.*124_*128del MANE Plus Clinical	NP_203524.1:n.*124_*128del