Canonical Allele Identifier: CA384149234
Gene: KRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25215545A>G , CM000674.2:g.25215545A>G GRCh38
NC_000012.11:g.25368479A>G , CM000674.1:g.25368479A>G GRCh37
NC_000012.10:g.25259746A>G NCBI36
NG_007524.1:g.40376T>C
NG_007524.2:g.40459T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256078.10:c.466T>C ENSP00000256078.5:p.Phe156Leu
ENST00000311936.8:c.451-5634T>C MANE Select ENSP00000308495.3:p.=
ENST00000256078.8:c.466T>C ENSP00000256078.4:p.Phe156Leu
ENST00000311936.7:c.451-5634T>C ENSP00000308495.3:p.=
ENST00000557334.5:c.112-5634T>C ENSP00000452512.1:p.=
NM_004985.4:c.451-5634T>C NP_004976.2:p.=
NM_033360.3:c.466T>C NP_203524.1:p.Phe156Leu
XM_006719069.2:c.466T>C XP_006719132.1:p.Phe156Leu
XM_011520653.1:c.451-5634T>C XP_011518955.1:p.=
XM_006719069.4:c.466T>C XP_006719132.1:p.Phe156Leu
XM_011520653.3:c.451-5634T>C XP_011518955.1:p.=
NM_001369786.1:c.466T>C NP_001356715.1:p.Phe156Leu
NM_001369787.1:c.451-5634T>C NP_001356716.1:p.=
NM_004985.5:c.451-5634T>C MANE Select NP_004976.2:p.=
NM_033360.4:c.466T>C NP_203524.1:p.Phe156Leu