Canonical Allele Identifier: CA603693299

Gene: KRAS

Linked Data

• gnomAD v2: 12-25378240-A-ATATATATATATG
• MyVariant Identifiers: chr12:g.25378240_25378241insTATATATATATG (hg19) ; chr12:g.25225306_25225307insTATATATATATG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225317_25225318insGTATATATATAT , CM000674.2:g.25225317_25225318insGTATATATATAT	GRCh38
NC_000012.11:g.25378251_25378252insGTATATATATAT , CM000674.1:g.25378251_25378252insGTATATATATAT	GRCh37
NC_000012.10:g.25269518_25269519insGTATATATATAT	NCBI36
NG_007524.1:g.30614_30615insCATATATATATA
NG_007524.2:g.30697_30698insCATATATATATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15396_112-15395insCATATATATATA	ENSP00000452512.1:n.112-15396_112-15395insCATATATATATA
ENST00000685328.1:c.450+307_450+308insCATATATATATA	ENSP00000508921.1:n.450+307_450+308insCATATATATATA
ENST00000686877.1:c.*421+307_*421+308insCATATATATATA	ENSP00000510431.1:n.*421+307_*421+308insCATATATATATA
ENST00000687356.1:c.*148+307_*148+308insCATATATATATA	ENSP00000510511.1:n.*148+307_*148+308insCATATATATATA
ENST00000688228.1:n.924+307_924+308insCATATATATATA
ENST00000688940.1:c.450+307_450+308insCATATATATATA	ENSP00000509238.1:n.450+307_450+308insCATATATATATA
ENST00000690406.1:c.160+307_160+308insCATATATATATA
ENST00000690804.1:c.*411+307_*411+308insCATATATATATA	ENSP00000508568.1:n.*411+307_*411+308insCATATATATATA
ENST00000692768.1:c.252+307_252+308insCATATATATATA	ENSP00000510254.1:n.252+307_252+308insCATATATATATA
ENST00000693229.1:c.375+307_375+308insCATATATATATA	ENSP00000509223.1:n.375+307_375+308insCATATATATATA
ENST00000256078.10:c.450+307_450+308insCATATATATATA MANE Plus Clinical	ENSP00000256078.5:n.450+307_450+308insCATATATATATA
ENST00000311936.8:c.450+307_450+308insCATATATATATA MANE Select	ENSP00000308495.3:n.450+307_450+308insCATATATATATA
ENST00000256078.8:c.450+307_450+308insCATATATATATA	ENSP00000256078.4:n.450+307_450+308insCATATATATATA
ENST00000311936.7:c.450+307_450+308insCATATATATATA	ENSP00000308495.3:n.450+307_450+308insCATATATATATA
ENST00000557334.5:c.112-15396_112-15395insCATATATATATA	ENSP00000452512.1:n.112-15396_112-15395insCATATATATATA
NM_004985.4:c.450+307_450+308insCATATATATATA	NP_004976.2:n.450+307_450+308insCATATATATATA
NM_033360.3:c.450+307_450+308insCATATATATATA	NP_203524.1:n.450+307_450+308insCATATATATATA
XM_006719069.2:c.450+307_450+308insCATATATATATA	XP_006719132.1:n.450+307_450+308insCATATATATATA
XM_011520653.1:c.450+307_450+308insCATATATATATA	XP_011518955.1:n.450+307_450+308insCATATATATATA
XM_006719069.4:c.450+307_450+308insCATATATATATA	XP_006719132.1:n.450+307_450+308insCATATATATATA
XM_011520653.3:c.450+307_450+308insCATATATATATA	XP_011518955.1:n.450+307_450+308insCATATATATATA
NM_001369786.1:c.450+307_450+308insCATATATATATA	NP_001356715.1:n.450+307_450+308insCATATATATATA
NM_001369787.1:c.450+307_450+308insCATATATATATA	NP_001356716.1:n.450+307_450+308insCATATATATATA
NM_004985.5:c.450+307_450+308insCATATATATATA MANE Select	NP_004976.2:n.450+307_450+308insCATATATATATA
NM_033360.4:c.450+307_450+308insCATATATATATA MANE Plus Clinical	NP_203524.1:n.450+307_450+308insCATATATATATA