Canonical Allele Identifier: CA686712265

Gene: KRAS ETFRF1

Linked Data

• dbSNP Id: rs1301653074
• MyVariant Identifiers: chr12:g.25359242_25359243insCATT (hg19) ; chr12:g.25206308_25206309insCATT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25206311_25206314dup , CM000674.2:g.25206311_25206314dup	GRCh38
NC_000012.11:g.25359245_25359248dup , CM000674.1:g.25359245_25359248dup	GRCh37
NC_000012.10:g.25250512_25250515dup	NCBI36
NG_007524.1:g.49609_49612dup
NG_007524.2:g.49692_49695dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*3483_*3486dup (KRAS)	ENSP00000508921.1:n.*3483_*3486dup
ENST00000686877.1:c.*4021_*4024dup (KRAS)	ENSP00000510431.1:n.*4021_*4024dup
ENST00000687356.1:c.*3748_*3751dup (KRAS)	ENSP00000510511.1:n.*3748_*3751dup
ENST00000690406.1:c.3853_3856dup (KRAS)
ENST00000692768.1:c.*3483_*3486dup (KRAS)	ENSP00000510254.1:n.*3483_*3486dup
ENST00000693229.1:c.*3483_*3486dup (KRAS)	ENSP00000509223.1:n.*3483_*3486dup
ENST00000256078.10:c.*3604_*3607dup (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*3604_*3607dup
ENST00000311936.8:c.*3483_*3486dup (KRAS) MANE Select	ENSP00000308495.3:n.*3483_*3486dup
ENST00000553788.6:c.51+2304_51+2307dup (ETFRF1)	ENSP00000451938.2:n.51+2304_51+2307dup
ENST00000311936.7:c.*3483_*3486dup (KRAS)	ENSP00000308495.3:n.*3483_*3486dup
ENST00000553788.5:c.45+2304_45+2307dup (ETFRF1)	ENSP00000451938.1:n.45+2304_45+2307dup
NM_004985.4:c.*3483_*3486dup (KRAS)	NP_004976.2:n.*3483_*3486dup
NM_033360.3:c.*3604_*3607dup (KRAS)	NP_203524.1:n.*3604_*3607dup
XM_011520653.1:c.*3483_*3486dup (KRAS)	XP_011518955.1:n.*3483_*3486dup
XM_011520653.3:c.*3483_*3486dup (KRAS)	XP_011518955.1:n.*3483_*3486dup
NM_001369786.1:c.*3604_*3607dup (KRAS)	NP_001356715.1:n.*3604_*3607dup
NM_001369787.1:c.*3483_*3486dup (KRAS)	NP_001356716.1:n.*3483_*3486dup
NM_004985.5:c.*3483_*3486dup (KRAS) MANE Select	NP_004976.2:n.*3483_*3486dup
NM_033360.4:c.*3604_*3607dup (KRAS) MANE Plus Clinical	NP_203524.1:n.*3604_*3607dup