Canonical Allele Identifier: CA686714716
Gene: KRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 931154
ClinVar RCV Id: RCV001197454
dbSNP Id: rs1373386042
gnomAD v3: 12-25209825-CTTT-C
gnomAD v4: 12-25209825-CTTT-C
MyVariant Identifiers: chr12:g.25362760_25362762del (hg19) chr12:g.25209826_25209828del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209828_25209830del , CM000674.2:g.25209828_25209830del GRCh38
NC_000012.11:g.25362762_25362764del , CM000674.1:g.25362762_25362764del GRCh37
NC_000012.10:g.25254029_25254031del NCBI36
NG_007524.1:g.46093_46095del
NG_007524.2:g.46176_46178del

Transcript Alleles

HGVS Amino-acid Change
ENST00000557334.6:c.195_197del ENSP00000452512.1:p.Lys66del
ENST00000685328.1:c.534_536del ENSP00000508921.1:p.Lys179del
ENST00000686877.1:c.*505_*507del ENSP00000510431.1:n.*505_*507del
ENST00000687356.1:c.*232_*234del ENSP00000510511.1:n.*232_*234del
ENST00000688228.1:n.1008_1010del
ENST00000688940.1:c.534_536del ENSP00000509238.1:p.Lys179del
ENST00000690406.1:c.337_339del
ENST00000690804.1:c.*495_*497del ENSP00000508568.1:n.*495_*497del
ENST00000692768.1:c.336_338del ENSP00000510254.1:p.Lys113del
ENST00000693229.1:c.459_461del ENSP00000509223.1:p.Lys154del
ENST00000256078.10:c.*88_*90del MANE Plus Clinical ENSP00000256078.5:n.*88_*90del
ENST00000311936.8:c.534_536del MANE Select ENSP00000308495.3:p.Lys179del
ENST00000256078.8:c.*88_*90del ENSP00000256078.4:n.*88_*90del
ENST00000311936.7:c.534_536del ENSP00000308495.3:p.Lys179del
ENST00000557334.5:c.195_197del ENSP00000452512.1:p.Lys66del
NM_004985.4:c.534_536del NP_004976.2:p.Lys179del
NM_033360.3:c.*88_*90del NP_203524.1:n.*88_*90del
XM_006719069.2:c.*88_*90del XP_006719132.1:n.*88_*90del
XM_011520653.1:c.534_536del XP_011518955.1:p.Lys179del
XM_006719069.4:c.*88_*90del XP_006719132.1:n.*88_*90del
XM_011520653.3:c.534_536del XP_011518955.1:p.Lys179del
NM_001369786.1:c.*88_*90del NP_001356715.1:n.*88_*90del
NM_001369787.1:c.534_536del NP_001356716.1:p.Lys179del
NM_004985.5:c.534_536del MANE Select NP_004976.2:p.Lys179del
NM_033360.4:c.*88_*90del MANE Plus Clinical NP_203524.1:n.*88_*90del
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