Canonical Allele Identifier: CA135584
Gene: KRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 45129
ClinVar RCV Id: RCV000038278 RCV000465001 RCV000513996 RCV001813343 RCV004018867 RCV004549455
dbSNP Id: rs397517043
ExAC: 12:25362762 TTTC / T
gnomAD v2: 12-25362762-TTTC-T
gnomAD v3: 12-25209828-TTTC-T
gnomAD v4: 12-25209828-TTTC-T
MyVariant Identifiers: chr12:g.25362763_25362765del (hg19) chr12:g.25209829_25209831del (hg38)
ERepo: CA135584/MONDO:0021060/004
PubMed: PMID:24728327
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209834_25209836del , CM000674.2:g.25209834_25209836del GRCh38
NC_000012.11:g.25362768_25362770del , CM000674.1:g.25362768_25362770del GRCh37
NC_000012.10:g.25254035_25254037del NCBI36
NG_007524.1:g.46090_46092del
NG_007524.2:g.46173_46175del

Transcript Alleles

HGVS Amino-acid Change
ENST00000557334.6:c.192_194del ENSP00000452512.1:p.Lys65del
ENST00000685328.1:c.531_533del ENSP00000508921.1:p.Lys178del
ENST00000686877.1:c.*502_*504del ENSP00000510431.1:n.*502_*504del
ENST00000687356.1:c.*229_*231del ENSP00000510511.1:n.*229_*231del
ENST00000688228.1:n.1005_1007del
ENST00000688940.1:c.531_533del ENSP00000509238.1:p.Lys178del
ENST00000690406.1:c.334_336del
ENST00000690804.1:c.*492_*494del ENSP00000508568.1:n.*492_*494del
ENST00000692768.1:c.333_335del ENSP00000510254.1:p.Lys112del
ENST00000693229.1:c.456_458del ENSP00000509223.1:p.Lys153del
ENST00000256078.10:c.*85_*87del MANE Plus Clinical ENSP00000256078.5:n.*85_*87del
ENST00000311936.8:c.531_533del MANE Select ENSP00000308495.3:p.Lys178del
ENST00000256078.8:c.*85_*87del ENSP00000256078.4:n.*85_*87del
ENST00000311936.7:c.531_533del ENSP00000308495.3:p.Lys178del
ENST00000557334.5:c.192_194del ENSP00000452512.1:p.Lys65del
NM_004985.4:c.531_533del NP_004976.2:p.Lys178del
NM_033360.3:c.*85_*87del NP_203524.1:n.*85_*87del
XM_006719069.2:c.*85_*87del XP_006719132.1:n.*85_*87del
XM_011520653.1:c.531_533del XP_011518955.1:p.Lys178del
XM_006719069.4:c.*85_*87del XP_006719132.1:n.*85_*87del
XM_011520653.3:c.531_533del XP_011518955.1:p.Lys178del
NM_001369786.1:c.*85_*87del NP_001356715.1:n.*85_*87del
NM_001369787.1:c.531_533del NP_001356716.1:p.Lys178del
NM_004985.5:c.531_533del MANE Select NP_004976.2:p.Lys178del
NM_033360.4:c.*85_*87del MANE Plus Clinical NP_203524.1:n.*85_*87del
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