Canonical Allele Identifier: CA2022897984
Gene: KRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25245216_25245218delinsTTA , CM000674.2:g.25245216_25245218delinsTTA GRCh38
NC_000012.11:g.25398150_25398152delinsTTA , CM000674.1:g.25398150_25398152delinsTTA GRCh37
NC_000012.10:g.25289417_25289419delinsTTA NCBI36
NG_007524.1:g.10703_10705delinsTAA
NG_007524.2:g.10786_10788delinsTAA

Transcript Alleles

HGVS Amino-acid change
ENST00000256078.10:c.111+56_111+58delinsTAA ENSP00000256078.5:p.=
ENST00000311936.8:c.111+56_111+58delinsTAA MANE Select ENSP00000308495.3:p.=
ENST00000256078.8:c.111+56_111+58delinsTAA ENSP00000256078.4:p.=
ENST00000311936.7:c.111+56_111+58delinsTAA ENSP00000308495.3:p.=
ENST00000556131.1:c.111+56_111+58delinsTAA ENSP00000451856.1:p.=
ENST00000557334.5:c.111+56_111+58delinsTAA ENSP00000452512.1:p.=
NM_004985.4:c.111+56_111+58delinsTAA NP_004976.2:p.=
NM_033360.3:c.111+56_111+58delinsTAA NP_203524.1:p.=
XM_006719069.2:c.111+56_111+58delinsTAA XP_006719132.1:p.=
XM_011520653.1:c.111+56_111+58delinsTAA XP_011518955.1:p.=
XM_006719069.4:c.111+56_111+58delinsTAA XP_006719132.1:p.=
XM_011520653.3:c.111+56_111+58delinsTAA XP_011518955.1:p.=
NM_001369786.1:c.111+56_111+58delinsTAA NP_001356715.1:p.=
NM_001369787.1:c.111+56_111+58delinsTAA NP_001356716.1:p.=
NM_004985.5:c.111+56_111+58delinsTAA MANE Select NP_004976.2:p.=
NM_033360.4:c.111+56_111+58delinsTAA NP_203524.1:p.=