Canonical Allele Identifier: CA384148298
Gene: KRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209806C>G , CM000674.2:g.25209806C>G GRCh38
NC_000012.11:g.25362740C>G , CM000674.1:g.25362740C>G GRCh37
NC_000012.10:g.25254007C>G NCBI36
NG_007524.1:g.46115G>C
NG_007524.2:g.46198G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.217G>C ENSP00000452512.1:p.Val73Leu
ENST00000685328.1:c.556G>C ENSP00000508921.1:p.Val186Leu
ENST00000686877.1:c.*527G>C ENSP00000510431.1:n.*527G>C
ENST00000687356.1:c.*254G>C ENSP00000510511.1:n.*254G>C
ENST00000688228.1:n.1030G>C
ENST00000688940.1:c.556G>C ENSP00000509238.1:p.Val186Leu
ENST00000690406.1:c.359G>C
ENST00000690804.1:c.*517G>C ENSP00000508568.1:n.*517G>C
ENST00000692768.1:c.358G>C ENSP00000510254.1:p.Val120Leu
ENST00000693229.1:c.481G>C ENSP00000509223.1:p.Val161Leu
ENST00000256078.10:c.*110G>C MANE Plus Clinical ENSP00000256078.5:n.*110G>C
ENST00000311936.8:c.556G>C MANE Select ENSP00000308495.3:p.Val186Leu
ENST00000256078.8:c.*110G>C ENSP00000256078.4:n.*110G>C
ENST00000311936.7:c.556G>C ENSP00000308495.3:p.Val186Leu
ENST00000557334.5:c.217G>C ENSP00000452512.1:p.Val73Leu
NM_004985.4:c.556G>C NP_004976.2:p.Val186Leu
NM_033360.3:c.*110G>C NP_203524.1:n.*110G>C
XM_011520653.1:c.556G>C XP_011518955.1:p.Val186Leu
XM_011520653.3:c.556G>C XP_011518955.1:p.Val186Leu
NM_001369786.1:c.*110G>C NP_001356715.1:n.*110G>C
NM_001369787.1:c.556G>C NP_001356716.1:p.Val186Leu
NM_004985.5:c.556G>C MANE Select NP_004976.2:p.Val186Leu
NM_033360.4:c.*110G>C MANE Plus Clinical NP_203524.1:n.*110G>C