Canonical Allele Identifier: CA2517324544

Gene: KRAS ETFRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25207032_25207033insC , CM000674.2:g.25207032_25207033insC	GRCh38
NC_000012.11:g.25359966_25359967insC , CM000674.1:g.25359966_25359967insC	GRCh37
NC_000012.10:g.25251233_25251234insC	NCBI36
NG_007524.1:g.48888_48889insG
NG_007524.2:g.48971_48972insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000685328.1:c.*2762_*2763insG (KRAS)	ENSP00000508921.1:n.*2762_*2763insG
ENST00000686877.1:c.*3300_*3301insG (KRAS)	ENSP00000510431.1:n.*3300_*3301insG
ENST00000687356.1:c.*3027_*3028insG (KRAS)	ENSP00000510511.1:n.*3027_*3028insG
ENST00000688940.1:c.*2762_*2763insG (KRAS)	ENSP00000509238.1:n.*2762_*2763insG
ENST00000690406.1:c.3132_3133insG (KRAS)
ENST00000692768.1:c.*2762_*2763insG (KRAS)	ENSP00000510254.1:n.*2762_*2763insG
ENST00000693229.1:c.*2762_*2763insG (KRAS)	ENSP00000509223.1:n.*2762_*2763insG
ENST00000256078.10:c.*2883_*2884insG (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*2883_*2884insG
ENST00000311936.8:c.*2762_*2763insG (KRAS) MANE Select	ENSP00000308495.3:n.*2762_*2763insG
ENST00000553788.6:c.52-2163_52-2162insC (ETFRF1)	ENSP00000451938.2:n.52-2163_52-2162insC
ENST00000311936.7:c.*2762_*2763insG (KRAS)	ENSP00000308495.3:n.*2762_*2763insG
ENST00000553788.5:c.46-2163_46-2162insC (ETFRF1)	ENSP00000451938.1:n.46-2163_46-2162insC
NM_004985.4:c.*2762_*2763insG (KRAS)	NP_004976.2:n.*2762_*2763insG
NM_033360.3:c.*2883_*2884insG (KRAS)	NP_203524.1:n.*2883_*2884insG
XM_011520653.1:c.*2762_*2763insG (KRAS)	XP_011518955.1:n.*2762_*2763insG
XM_011520653.3:c.*2762_*2763insG (KRAS)	XP_011518955.1:n.*2762_*2763insG
NM_001369786.1:c.*2883_*2884insG (KRAS)	NP_001356715.1:n.*2883_*2884insG
NM_001369787.1:c.*2762_*2763insG (KRAS)	NP_001356716.1:n.*2762_*2763insG
NM_004985.5:c.*2762_*2763insG (KRAS) MANE Select	NP_004976.2:n.*2762_*2763insG
NM_033360.4:c.*2883_*2884insG (KRAS) MANE Plus Clinical	NP_203524.1:n.*2883_*2884insG