Canonical Allele Identifier: CA686712220

Gene: KRAS ETFRF1

Linked Data

• dbSNP Id: rs1158089947
• MyVariant Identifiers: chr12:g.25359162_25359163insTGA (hg19) ; chr12:g.25206228_25206229insTGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25206230_25206232dup , CM000674.2:g.25206230_25206232dup	GRCh38
NC_000012.11:g.25359164_25359166dup , CM000674.1:g.25359164_25359166dup	GRCh37
NC_000012.10:g.25250431_25250433dup	NCBI36
NG_007524.1:g.49690_49692dup
NG_007524.2:g.49773_49775dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*3564_*3566dup (KRAS)	ENSP00000508921.1:n.*3564_*3566dup
ENST00000686877.1:c.*4102_*4104dup (KRAS)	ENSP00000510431.1:n.*4102_*4104dup
ENST00000687356.1:c.*3829_*3831dup (KRAS)	ENSP00000510511.1:n.*3829_*3831dup
ENST00000690406.1:c.3934_3936dup (KRAS)
ENST00000692768.1:c.*3564_*3566dup (KRAS)	ENSP00000510254.1:n.*3564_*3566dup
ENST00000693229.1:c.*3564_*3566dup (KRAS)	ENSP00000509223.1:n.*3564_*3566dup
ENST00000256078.10:c.*3685_*3687dup (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*3685_*3687dup
ENST00000311936.8:c.*3564_*3566dup (KRAS) MANE Select	ENSP00000308495.3:n.*3564_*3566dup
ENST00000553788.6:c.51+2223_51+2225dup (ETFRF1)	ENSP00000451938.2:n.51+2223_51+2225dup
ENST00000311936.7:c.*3564_*3566dup (KRAS)	ENSP00000308495.3:n.*3564_*3566dup
ENST00000553788.5:c.45+2223_45+2225dup (ETFRF1)	ENSP00000451938.1:n.45+2223_45+2225dup
NM_004985.4:c.*3564_*3566dup (KRAS)	NP_004976.2:n.*3564_*3566dup
NM_033360.3:c.*3685_*3687dup (KRAS)	NP_203524.1:n.*3685_*3687dup
XM_011520653.1:c.*3564_*3566dup (KRAS)	XP_011518955.1:n.*3564_*3566dup
XM_011520653.3:c.*3564_*3566dup (KRAS)	XP_011518955.1:n.*3564_*3566dup
NM_001369786.1:c.*3685_*3687dup (KRAS)	NP_001356715.1:n.*3685_*3687dup
NM_001369787.1:c.*3564_*3566dup (KRAS)	NP_001356716.1:n.*3564_*3566dup
NM_004985.5:c.*3564_*3566dup (KRAS) MANE Select	NP_004976.2:n.*3564_*3566dup
NM_033360.4:c.*3685_*3687dup (KRAS) MANE Plus Clinical	NP_203524.1:n.*3685_*3687dup