Canonical Allele Identifier: CA2840633018
Gene: KRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209850_25209851insAGACTG , CM000674.2:g.25209850_25209851insAGACTG GRCh38
NC_000012.11:g.25362784_25362785insAGACTG , CM000674.1:g.25362784_25362785insAGACTG GRCh37
NC_000012.10:g.25254051_25254052insAGACTG NCBI36
NG_007524.1:g.46070_46071insCAGTCT
NG_007524.2:g.46153_46154insCAGTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000557334.6:c.172_173insCAGTCT ENSP00000452512.1:p.Ser58delinsThrValCys
ENST00000685328.1:c.511_512insCAGTCT ENSP00000508921.1:p.Ser171delinsThrValCys
ENST00000686877.1:c.*482_*483insCAGTCT ENSP00000510431.1:n.*482_*483insCAGTCT
ENST00000687356.1:c.*209_*210insCAGTCT ENSP00000510511.1:n.*209_*210insCAGTCT
ENST00000688228.1:n.985_986insCAGTCT
ENST00000688940.1:c.511_512insCAGTCT ENSP00000509238.1:p.Ser171delinsThrValCys
ENST00000690406.1:c.314_315insCAGTCT
ENST00000690804.1:c.*472_*473insCAGTCT ENSP00000508568.1:n.*472_*473insCAGTCT
ENST00000692768.1:c.313_314insCAGTCT ENSP00000510254.1:p.Ser105delinsThrValCys
ENST00000693229.1:c.436_437insCAGTCT ENSP00000509223.1:p.Ser146delinsThrValCys
ENST00000256078.10:c.*65_*66insCAGTCT MANE Plus Clinical ENSP00000256078.5:n.*65_*66insCAGTCT
ENST00000311936.8:c.511_512insCAGTCT MANE Select ENSP00000308495.3:p.Ser171delinsThrValCys
ENST00000256078.8:c.*65_*66insCAGTCT ENSP00000256078.4:n.*65_*66insCAGTCT
ENST00000311936.7:c.511_512insCAGTCT ENSP00000308495.3:p.Ser171delinsThrValCys
ENST00000557334.5:c.172_173insCAGTCT ENSP00000452512.1:p.Ser58delinsThrValCys
NM_004985.4:c.511_512insCAGTCT NP_004976.2:p.Ser171delinsThrValCys
NM_033360.3:c.*65_*66insCAGTCT NP_203524.1:n.*65_*66insCAGTCT
XM_006719069.2:c.*65_*66insCAGTCT XP_006719132.1:n.*65_*66insCAGTCT
XM_011520653.1:c.511_512insCAGTCT XP_011518955.1:p.Ser171delinsThrValCys
XM_006719069.4:c.*65_*66insCAGTCT XP_006719132.1:n.*65_*66insCAGTCT
XM_011520653.3:c.511_512insCAGTCT XP_011518955.1:p.Ser171delinsThrValCys
NM_001369786.1:c.*65_*66insCAGTCT NP_001356715.1:n.*65_*66insCAGTCT
NM_001369787.1:c.511_512insCAGTCT NP_001356716.1:p.Ser171delinsThrValCys
NM_004985.5:c.511_512insCAGTCT MANE Select NP_004976.2:p.Ser171delinsThrValCys
NM_033360.4:c.*65_*66insCAGTCT MANE Plus Clinical NP_203524.1:n.*65_*66insCAGTCT