Canonical Allele Identifier: CA686718069

Gene: KRAS

Linked Data

• dbSNP Id: rs1290695979
• MyVariant Identifiers: chr12:g.25368319_25368320insA (hg19) ; chr12:g.25215385_25215386insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25215385_25215386insA , CM000674.2:g.25215385_25215386insA	GRCh38
NC_000012.11:g.25368319_25368320insA , CM000674.1:g.25368319_25368320insA	GRCh37
NC_000012.10:g.25259586_25259587insA	NCBI36
NG_007524.1:g.40535_40536insT
NG_007524.2:g.40618_40619insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-5475_112-5474insT	ENSP00000452512.1:n.112-5475_112-5474insT
ENST00000685328.1:c.451-5475_451-5474insT	ENSP00000508921.1:n.451-5475_451-5474insT
ENST00000686877.1:c.*422-5475_*422-5474insT	ENSP00000510431.1:n.*422-5475_*422-5474insT
ENST00000687356.1:c.*149-5475_*149-5474insT	ENSP00000510511.1:n.*149-5475_*149-5474insT
ENST00000688228.1:n.925-5475_925-5474insT
ENST00000688940.1:c.451-5475_451-5474insT	ENSP00000509238.1:n.451-5475_451-5474insT
ENST00000690406.1:c.161-2180_161-2179insT
ENST00000690804.1:c.*412-5475_*412-5474insT	ENSP00000508568.1:n.*412-5475_*412-5474insT
ENST00000692768.1:c.253-5475_253-5474insT	ENSP00000510254.1:n.253-5475_253-5474insT
ENST00000693229.1:c.376-5475_376-5474insT	ENSP00000509223.1:n.376-5475_376-5474insT
ENST00000256078.10:c.*4+51_*4+52insT MANE Plus Clinical	ENSP00000256078.5:n.*4+51_*4+52insT
ENST00000311936.8:c.451-5475_451-5474insT MANE Select	ENSP00000308495.3:n.451-5475_451-5474insT
ENST00000256078.8:c.*4+51_*4+52insT	ENSP00000256078.4:n.*4+51_*4+52insT
ENST00000311936.7:c.451-5475_451-5474insT	ENSP00000308495.3:n.451-5475_451-5474insT
ENST00000557334.5:c.112-5475_112-5474insT	ENSP00000452512.1:n.112-5475_112-5474insT
NM_004985.4:c.451-5475_451-5474insT	NP_004976.2:n.451-5475_451-5474insT
NM_033360.3:c.*4+51_*4+52insT	NP_203524.1:n.*4+51_*4+52insT
XM_006719069.2:c.*4+51_*4+52insT	XP_006719132.1:n.*4+51_*4+52insT
XM_011520653.1:c.451-5475_451-5474insT	XP_011518955.1:n.451-5475_451-5474insT
XM_006719069.4:c.*4+51_*4+52insT	XP_006719132.1:n.*4+51_*4+52insT
XM_011520653.3:c.451-5475_451-5474insT	XP_011518955.1:n.451-5475_451-5474insT
NM_001369786.1:c.*4+51_*4+52insT	NP_001356715.1:n.*4+51_*4+52insT
NM_001369787.1:c.451-5475_451-5474insT	NP_001356716.1:n.451-5475_451-5474insT
NM_004985.5:c.451-5475_451-5474insT MANE Select	NP_004976.2:n.451-5475_451-5474insT
NM_033360.4:c.*4+51_*4+52insT MANE Plus Clinical	NP_203524.1:n.*4+51_*4+52insT