Canonical Allele Identifier: CA10632454
Gene: KRAS HGNC NCBI
ETFRF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 308062
ClinVar RCV Id: RCV000323439 RCV000380266
dbSNP Id: rs34719539
gnomAD v2: 12-25358662-CTT-C
gnomAD v3: 12-25205728-CTT-C
gnomAD v4: 12-25205728-CTT-C
COSMIC: COSN20109361 COSN20109362
MyVariant Identifiers: chr12:g.25358663_25358664del (hg19) chr12:g.25205729_25205730del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25205735_25205736del , CM000674.2:g.25205735_25205736del GRCh38
NC_000012.11:g.25358669_25358670del , CM000674.1:g.25358669_25358670del GRCh37
NC_000012.10:g.25249936_25249937del NCBI36
NG_007524.1:g.50191_50192del
NG_007524.2:g.50274_50275del

Transcript Alleles

HGVS Amino-acid Change
ENST00000685328.1:c.*4065_*4066del (KRAS) ENSP00000508921.1:n.*4065_*4066del
ENST00000686877.1:c.*4603_*4604del (KRAS) ENSP00000510431.1:n.*4603_*4604del
ENST00000687356.1:c.*4330_*4331del (KRAS) ENSP00000510511.1:n.*4330_*4331del
ENST00000690406.1:c.4435_4436del (KRAS)
ENST00000692768.1:c.*4065_*4066del (KRAS) ENSP00000510254.1:n.*4065_*4066del
ENST00000693229.1:c.*4065_*4066del (KRAS) ENSP00000509223.1:n.*4065_*4066del
ENST00000256078.10:c.*4186_*4187del (KRAS) MANE Plus Clinical ENSP00000256078.5:n.*4186_*4187del
ENST00000311936.8:c.*4065_*4066del (KRAS) MANE Select ENSP00000308495.3:n.*4065_*4066del
ENST00000553788.6:c.51+1728_51+1729del (ETFRF1) ENSP00000451938.2:n.51+1728_51+1729del
ENST00000311936.7:c.*4065_*4066del (KRAS) ENSP00000308495.3:n.*4065_*4066del
ENST00000553788.5:c.45+1728_45+1729del (ETFRF1) ENSP00000451938.1:n.45+1728_45+1729del
NM_004985.4:c.*4065_*4066del (KRAS) NP_004976.2:n.*4065_*4066del
NM_033360.3:c.*4186_*4187del (KRAS) NP_203524.1:n.*4186_*4187del
XM_011520653.1:c.*4065_*4066del (KRAS) XP_011518955.1:n.*4065_*4066del
XM_011520653.3:c.*4065_*4066del (KRAS) XP_011518955.1:n.*4065_*4066del
NM_001369786.1:c.*4186_*4187del (KRAS) NP_001356715.1:n.*4186_*4187del
NM_001369787.1:c.*4065_*4066del (KRAS) NP_001356716.1:n.*4065_*4066del
NM_004985.5:c.*4065_*4066del (KRAS) MANE Select NP_004976.2:n.*4065_*4066del
NM_033360.4:c.*4186_*4187del (KRAS) MANE Plus Clinical NP_203524.1:n.*4186_*4187del
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