Canonical Allele Identifier: CA384148511
Gene: KRAS HGNC NCBI

Linked Data

COSMIC: COSM327842

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209896A>G , CM000674.2:g.25209896A>G GRCh38
NC_000012.11:g.25362830A>G , CM000674.1:g.25362830A>G GRCh37
NC_000012.10:g.25254097A>G NCBI36
NG_007524.1:g.46025T>C
NG_007524.2:g.46108T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.127T>C ENSP00000452512.1:p.Phe43Leu
ENST00000685328.1:c.466T>C ENSP00000508921.1:p.Phe156Leu
ENST00000686877.1:c.*437T>C ENSP00000510431.1:n.*437T>C
ENST00000687356.1:c.*164T>C ENSP00000510511.1:n.*164T>C
ENST00000688228.1:n.940T>C
ENST00000688940.1:c.466T>C ENSP00000509238.1:p.Phe156Leu
ENST00000690406.1:n.269T>C
ENST00000690804.1:c.*427T>C ENSP00000508568.1:n.*427T>C
ENST00000692768.1:c.268T>C ENSP00000510254.1:p.Phe90Leu
ENST00000693229.1:c.391T>C ENSP00000509223.1:p.Phe131Leu
ENST00000256078.10:c.*20T>C ENSP00000256078.5:n.*20T>C
ENST00000311936.8:c.466T>C MANE Select ENSP00000308495.3:p.Phe156Leu
ENST00000256078.8:c.*20T>C ENSP00000256078.4:n.*20T>C
ENST00000311936.7:c.466T>C ENSP00000308495.3:p.Phe156Leu
ENST00000557334.5:c.127T>C ENSP00000452512.1:p.Phe43Leu
NM_004985.4:c.466T>C NP_004976.2:p.Phe156Leu
NM_033360.3:c.*20T>C NP_203524.1:n.*20T>C
XM_006719069.2:c.*20T>C XP_006719132.1:n.*20T>C
XM_011520653.1:c.466T>C XP_011518955.1:p.Phe156Leu
XM_006719069.4:c.*20T>C XP_006719132.1:n.*20T>C
XM_011520653.3:c.466T>C XP_011518955.1:p.Phe156Leu
NM_001369786.1:c.*20T>C NP_001356715.1:n.*20T>C
NM_001369787.1:c.466T>C NP_001356716.1:p.Phe156Leu
NM_004985.5:c.466T>C MANE Select NP_004976.2:p.Phe156Leu
NM_033360.4:c.*20T>C NP_203524.1:n.*20T>C