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
ENST00000557334.6:c.112-5634T>C ENSP00000452512.1:n.112-5634T>C
ENST00000685328.1:c.451-5634T>C ENSP00000508921.1:n.451-5634T>C
ENST00000686877.1:c.*422-5634T>C ENSP00000510431.1:n.*422-5634T>C
ENST00000687356.1:c.*149-5634T>C ENSP00000510511.1:n.*149-5634T>C
ENST00000688228.1:n.925-5634T>C
ENST00000688940.1:c.451-5634T>C ENSP00000509238.1:n.451-5634T>C
ENST00000690406.1:n.161-2339T>C
ENST00000690804.1:c.*412-5634T>C ENSP00000508568.1:n.*412-5634T>C
ENST00000692768.1:c.253-5634T>C ENSP00000510254.1:n.253-5634T>C
ENST00000693229.1:c.376-5634T>C ENSP00000509223.1:n.376-5634T>C
ENST00000256078.10:c.466T>C ENSP00000256078.5:p.Phe156Leu
ENST00000311936.8:c.451-5634T>C MANE Select ENSP00000308495.3:n.451-5634T>C
ENST00000256078.8:c.466T>C ENSP00000256078.4:p.Phe156Leu
ENST00000311936.7:c.451-5634T>C ENSP00000308495.3:n.451-5634T>C
ENST00000557334.5:c.112-5634T>C ENSP00000452512.1:n.112-5634T>C
NM_004985.4:c.451-5634T>C NP_004976.2:n.451-5634T>C
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:n.451-5634T>C
XM_006719069.4:c.466T>C XP_006719132.1:p.Phe156Leu
XM_011520653.3:c.451-5634T>C XP_011518955.1:n.451-5634T>C
NM_001369786.1:c.466T>C NP_001356715.1:p.Phe156Leu
NM_001369787.1:c.451-5634T>C NP_001356716.1:n.451-5634T>C
NM_004985.5:c.451-5634T>C MANE Select NP_004976.2:n.451-5634T>C
NM_033360.4:c.466T>C NP_203524.1:p.Phe156Leu