Canonical Allele Identifier: CA2022897944
Gene: KRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25245185T= , CM000674.2:g.25245185T= GRCh38
NC_000012.11:g.25398119T= , CM000674.1:g.25398119T= GRCh37
NC_000012.10:g.25289386T= NCBI36
NG_007524.1:g.10736A=
NG_007524.2:g.10819A=

Transcript Alleles

HGVS Amino-acid change
ENST00000256078.10:c.111+89A= ENSP00000256078.5:p.=
ENST00000311936.8:c.111+89A= MANE Select ENSP00000308495.3:p.=
ENST00000256078.8:c.111+89A= ENSP00000256078.4:p.=
ENST00000311936.7:c.111+89A= ENSP00000308495.3:p.=
ENST00000556131.1:c.111+89A= ENSP00000451856.1:p.=
ENST00000557334.5:c.111+89A= ENSP00000452512.1:p.=
NM_004985.4:c.111+89A= NP_004976.2:p.=
NM_033360.3:c.111+89A= NP_203524.1:p.=
XM_006719069.2:c.111+89A= XP_006719132.1:p.=
XM_011520653.1:c.111+89A= XP_011518955.1:p.=
XM_006719069.4:c.111+89A= XP_006719132.1:p.=
XM_011520653.3:c.111+89A= XP_011518955.1:p.=
NM_001369786.1:c.111+89A= NP_001356715.1:p.=
NM_001369787.1:c.111+89A= NP_001356716.1:p.=
NM_004985.5:c.111+89A= MANE Select NP_004976.2:p.=
NM_033360.4:c.111+89A= NP_203524.1:p.=