Canonical Allele Identifier: CA10640714

Linked Data

ClinVar Variation Id: 308081
dbSNP Id: rs886049184

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25206824_25206827del , CM000674.2:g.25206824_25206827del GRCh38
NC_000012.11:g.25359758_25359761del , CM000674.1:g.25359758_25359761del GRCh37
NC_000012.10:g.25251025_25251028del NCBI36
NG_007524.1:g.49097_49100del
NG_007524.2:g.49180_49183del

Transcript Alleles

HGVS Amino-acid Change
ENST00000685328.1:c.*2971_*2974del (KRAS) ENSP00000508921.1:n.*2971_*2974del
ENST00000686877.1:c.*3509_*3512del (KRAS) ENSP00000510431.1:n.*3509_*3512del
ENST00000687356.1:c.*3236_*3239del (KRAS) ENSP00000510511.1:n.*3236_*3239del
ENST00000690406.1:c.3341_3344del (KRAS)
ENST00000692768.1:c.*2971_*2974del (KRAS) ENSP00000510254.1:n.*2971_*2974del
ENST00000693229.1:c.*2971_*2974del (KRAS) ENSP00000509223.1:n.*2971_*2974del
ENST00000256078.10:c.*3092_*3095del (KRAS) MANE Plus Clinical ENSP00000256078.5:n.*3092_*3095del
ENST00000311936.8:c.*2971_*2974del (KRAS) MANE Select ENSP00000308495.3:n.*2971_*2974del
ENST00000553788.6:c.52-2371_52-2368del (ETFRF1) ENSP00000451938.2:n.52-2371_52-2368del
ENST00000311936.7:c.*2971_*2974del (KRAS) ENSP00000308495.3:n.*2971_*2974del
ENST00000553788.5:c.46-2371_46-2368del (ETFRF1) ENSP00000451938.1:n.46-2371_46-2368del
NM_004985.4:c.*2971_*2974del (KRAS) NP_004976.2:n.*2971_*2974del
NM_033360.3:c.*3092_*3095del (KRAS) NP_203524.1:n.*3092_*3095del
XM_011520653.1:c.*2971_*2974del (KRAS) XP_011518955.1:n.*2971_*2974del
XM_011520653.3:c.*2971_*2974del (KRAS) XP_011518955.1:n.*2971_*2974del
NM_001369786.1:c.*3092_*3095del (KRAS) NP_001356715.1:n.*3092_*3095del
NM_001369787.1:c.*2971_*2974del (KRAS) NP_001356716.1:n.*2971_*2974del
NM_004985.5:c.*2971_*2974del (KRAS) MANE Select NP_004976.2:n.*2971_*2974del
NM_033360.4:c.*3092_*3095del (KRAS) MANE Plus Clinical NP_203524.1:n.*3092_*3095del