Canonical Allele Identifier: CA686718321

Gene: KRAS

Linked Data

• dbSNP Id: rs1162819760
• MyVariant Identifiers: chr12:g.25368485_25368486insT (hg19) ; chr12:g.25215551_25215552insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25215551_25215552insT , CM000674.2:g.25215551_25215552insT	GRCh38
NC_000012.11:g.25368485_25368486insT , CM000674.1:g.25368485_25368486insT	GRCh37
NC_000012.10:g.25259752_25259753insT	NCBI36
NG_007524.1:g.40369_40370insA
NG_007524.2:g.40452_40453insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-5641_112-5640insA	ENSP00000452512.1:n.112-5641_112-5640insA...
ENST00000685328.1:c.451-5641_451-5640insA	ENSP00000508921.1:n.451-5641_451-5640insA...
ENST00000686877.1:c.*422-5641_*422-5640insA	ENSP00000510431.1:n.*422-5641_*422-5640in...
ENST00000687356.1:c.*149-5641_*149-5640insA	ENSP00000510511.1:n.*149-5641_*149-5640in...
ENST00000688228.1:n.925-5641_925-5640insA
ENST00000688940.1:c.451-5641_451-5640insA	ENSP00000509238.1:n.451-5641_451-5640insA...
ENST00000690406.1:c.161-2346_161-2345insA
ENST00000690804.1:c.*412-5641_*412-5640insA	ENSP00000508568.1:n.*412-5641_*412-5640in...
ENST00000692768.1:c.253-5641_253-5640insA	ENSP00000510254.1:n.253-5641_253-5640insA...
ENST00000693229.1:c.376-5641_376-5640insA	ENSP00000509223.1:n.376-5641_376-5640insA...
ENST00000256078.10:c.459_460insA MANE Plus Clinical	ENSP00000256078.5:p.Asp154ArgfsTer?
ENST00000311936.8:c.451-5641_451-5640insA MANE Select	ENSP00000308495.3:n.451-5641_451-5640insA...
ENST00000256078.8:c.459_460insA	ENSP00000256078.4:p.Asp154ArgfsTer?
ENST00000311936.7:c.451-5641_451-5640insA	ENSP00000308495.3:n.451-5641_451-5640insA...
ENST00000557334.5:c.112-5641_112-5640insA	ENSP00000452512.1:n.112-5641_112-5640insA...
NM_004985.4:c.451-5641_451-5640insA	NP_004976.2:n.451-5641_451-5640insA
NM_033360.3:c.459_460insA	NP_203524.1:p.Asp154ArgfsTer?
XM_006719069.2:c.459_460insA	XP_006719132.1:p.Asp154ArgfsTer?
XM_011520653.1:c.451-5641_451-5640insA	XP_011518955.1:n.451-5641_451-5640insA
XM_006719069.4:c.459_460insA	XP_006719132.1:p.Asp154ArgfsTer?
XM_011520653.3:c.451-5641_451-5640insA	XP_011518955.1:n.451-5641_451-5640insA
NM_001369786.1:c.459_460insA	NP_001356715.1:p.Asp154ArgfsTer?
NM_001369787.1:c.451-5641_451-5640insA	NP_001356716.1:n.451-5641_451-5640insA
NM_004985.5:c.451-5641_451-5640insA MANE Select	NP_004976.2:n.451-5641_451-5640insA
NM_033360.4:c.459_460insA MANE Plus Clinical	NP_203524.1:p.Asp154ArgfsTer?