Canonical Allele Identifier: CA2022880695

Gene: KRAS ETFRF1

Linked Data

• dbSNP Id: rs1951133643

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25205946_25205951del , CM000674.2:g.25205946_25205951del	GRCh38
NC_000012.11:g.25358880_25358885del , CM000674.1:g.25358880_25358885del	GRCh37
NC_000012.10:g.25250147_25250152del	NCBI36
NG_007524.1:g.49975_49980del
NG_007524.2:g.50058_50063del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*3849_*3854del (KRAS)	ENSP00000508921.1:n.*3849_*3854del
ENST00000686877.1:c.*4387_*4392del (KRAS)	ENSP00000510431.1:n.*4387_*4392del
ENST00000687356.1:c.*4114_*4119del (KRAS)	ENSP00000510511.1:n.*4114_*4119del
ENST00000690406.1:c.4219_4224del (KRAS)
ENST00000692768.1:c.*3849_*3854del (KRAS)	ENSP00000510254.1:n.*3849_*3854del
ENST00000693229.1:c.*3849_*3854del (KRAS)	ENSP00000509223.1:n.*3849_*3854del
ENST00000256078.10:c.*3970_*3975del (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*3970_*3975del
ENST00000311936.8:c.*3849_*3854del (KRAS) MANE Select	ENSP00000308495.3:n.*3849_*3854del
ENST00000553788.6:c.51+1939_51+1944del (ETFRF1)	ENSP00000451938.2:n.51+1939_51+1944del
ENST00000311936.7:c.*3849_*3854del (KRAS)	ENSP00000308495.3:n.*3849_*3854del
ENST00000553788.5:c.45+1939_45+1944del (ETFRF1)	ENSP00000451938.1:n.45+1939_45+1944del
NM_004985.4:c.*3849_*3854del (KRAS)	NP_004976.2:n.*3849_*3854del
NM_033360.3:c.*3970_*3975del (KRAS)	NP_203524.1:n.*3970_*3975del
XM_011520653.1:c.*3849_*3854del (KRAS)	XP_011518955.1:n.*3849_*3854del
XM_011520653.3:c.*3849_*3854del (KRAS)	XP_011518955.1:n.*3849_*3854del
NM_001369786.1:c.*3970_*3975del (KRAS)	NP_001356715.1:n.*3970_*3975del
NM_001369787.1:c.*3849_*3854del (KRAS)	NP_001356716.1:n.*3849_*3854del
NM_004985.5:c.*3849_*3854del (KRAS) MANE Select	NP_004976.2:n.*3849_*3854del
NM_033360.4:c.*3970_*3975del (KRAS) MANE Plus Clinical	NP_203524.1:n.*3970_*3975del