Canonical Allele Identifier: CA686712249

Gene: KRAS ETFRF1

Linked Data

• dbSNP Id: rs1283426013
• gnomAD v3: 12-25206280-A-AAAT
• gnomAD v4: 12-25206280-A-AAAT
• MyVariant Identifiers: chr12:g.25359214_25359215insAAT (hg19) ; chr12:g.25206280_25206281insAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25206282_25206284dup , CM000674.2:g.25206282_25206284dup	GRCh38
NC_000012.11:g.25359216_25359218dup , CM000674.1:g.25359216_25359218dup	GRCh37
NC_000012.10:g.25250483_25250485dup	NCBI36
NG_007524.1:g.49638_49640dup
NG_007524.2:g.49721_49723dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*3512_*3514dup (KRAS)	ENSP00000508921.1:n.*3512_*3514dup
ENST00000686877.1:c.*4050_*4052dup (KRAS)	ENSP00000510431.1:n.*4050_*4052dup
ENST00000687356.1:c.*3777_*3779dup (KRAS)	ENSP00000510511.1:n.*3777_*3779dup
ENST00000690406.1:c.3882_3884dup (KRAS)
ENST00000692768.1:c.*3512_*3514dup (KRAS)	ENSP00000510254.1:n.*3512_*3514dup
ENST00000693229.1:c.*3512_*3514dup (KRAS)	ENSP00000509223.1:n.*3512_*3514dup
ENST00000256078.10:c.*3633_*3635dup (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*3633_*3635dup
ENST00000311936.8:c.*3512_*3514dup (KRAS) MANE Select	ENSP00000308495.3:n.*3512_*3514dup
ENST00000553788.6:c.51+2275_51+2277dup (ETFRF1)	ENSP00000451938.2:n.51+2275_51+2277dup
ENST00000311936.7:c.*3512_*3514dup (KRAS)	ENSP00000308495.3:n.*3512_*3514dup
ENST00000553788.5:c.45+2275_45+2277dup (ETFRF1)	ENSP00000451938.1:n.45+2275_45+2277dup
NM_004985.4:c.*3512_*3514dup (KRAS)	NP_004976.2:n.*3512_*3514dup
NM_033360.3:c.*3633_*3635dup (KRAS)	NP_203524.1:n.*3633_*3635dup
XM_011520653.1:c.*3512_*3514dup (KRAS)	XP_011518955.1:n.*3512_*3514dup
XM_011520653.3:c.*3512_*3514dup (KRAS)	XP_011518955.1:n.*3512_*3514dup
NM_001369786.1:c.*3633_*3635dup (KRAS)	NP_001356715.1:n.*3633_*3635dup
NM_001369787.1:c.*3512_*3514dup (KRAS)	NP_001356716.1:n.*3512_*3514dup
NM_004985.5:c.*3512_*3514dup (KRAS) MANE Select	NP_004976.2:n.*3512_*3514dup
NM_033360.4:c.*3633_*3635dup (KRAS) MANE Plus Clinical	NP_203524.1:n.*3633_*3635dup