Canonical Allele Identifier: CA2022884554
Gene: KRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209822_25209826delinsCTTCT , CM000674.2:g.25209822_25209826delinsCTTCT GRCh38
NC_000012.11:g.25362756_25362760delinsCTTCT , CM000674.1:g.25362756_25362760delinsCTTCT GRCh37
NC_000012.10:g.25254023_25254027delinsCTTCT NCBI36
NG_007524.1:g.46095_46099delinsAGAAG
NG_007524.2:g.46178_46182delinsAGAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000557334.6:c.197_201delinsAGAAG ENSP00000452512.1:p.Lys66=
ENST00000685328.1:c.536_540delinsAGAAG ENSP00000508921.1:p.Lys179=
ENST00000686877.1:c.*507_*511delinsAGAAG ENSP00000510431.1:n.*507_*511delinsAGAAG
ENST00000687356.1:c.*234_*238delinsAGAAG ENSP00000510511.1:n.*234_*238delinsAGAAG
ENST00000688228.1:n.1010_1014delinsAGAAG
ENST00000688940.1:c.536_540delinsAGAAG ENSP00000509238.1:p.Lys179=
ENST00000690406.1:c.339_343delinsAGAAG
ENST00000690804.1:c.*497_*501delinsAGAAG ENSP00000508568.1:n.*497_*501delinsAGAAG
ENST00000692768.1:c.338_342delinsAGAAG ENSP00000510254.1:p.Lys113=
ENST00000693229.1:c.461_465delinsAGAAG ENSP00000509223.1:p.Lys154=
ENST00000256078.10:c.*90_*94delinsAGAAG MANE Plus Clinical ENSP00000256078.5:n.*90_*94delinsAGAAG
ENST00000311936.8:c.536_540delinsAGAAG MANE Select ENSP00000308495.3:p.Lys179=
ENST00000256078.8:c.*90_*94delinsAGAAG ENSP00000256078.4:n.*90_*94delinsAGAAG
ENST00000311936.7:c.536_540delinsAGAAG ENSP00000308495.3:p.Lys179=
ENST00000557334.5:c.197_201delinsAGAAG ENSP00000452512.1:p.Lys66=
NM_004985.4:c.536_540delinsAGAAG NP_004976.2:p.Lys179=
NM_033360.3:c.*90_*94delinsAGAAG NP_203524.1:n.*90_*94delinsAGAAG
XM_011520653.1:c.536_540delinsAGAAG XP_011518955.1:p.Lys179=
XM_011520653.3:c.536_540delinsAGAAG XP_011518955.1:p.Lys179=
NM_001369786.1:c.*90_*94delinsAGAAG NP_001356715.1:n.*90_*94delinsAGAAG
NM_001369787.1:c.536_540delinsAGAAG NP_001356716.1:p.Lys179=
NM_004985.5:c.536_540delinsAGAAG MANE Select NP_004976.2:p.Lys179=
NM_033360.4:c.*90_*94delinsAGAAG MANE Plus Clinical NP_203524.1:n.*90_*94delinsAGAAG