Canonical Allele Identifier: CA384148281
Gene: KRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209798C>A , CM000674.2:g.25209798C>A GRCh38
NC_000012.11:g.25362732C>A , CM000674.1:g.25362732C>A GRCh37
NC_000012.10:g.25253999C>A NCBI36
NG_007524.1:g.46123G>T
NG_007524.2:g.46206G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.225G>T ENSP00000452512.1:p.Met75Ile
ENST00000685328.1:c.564G>T ENSP00000508921.1:p.Met188Ile
ENST00000686877.1:c.*535G>T ENSP00000510431.1:n.*535G>T
ENST00000687356.1:c.*262G>T ENSP00000510511.1:n.*262G>T
ENST00000688228.1:n.1038G>T
ENST00000688940.1:c.564G>T ENSP00000509238.1:p.Met188Ile
ENST00000690406.1:c.367G>T
ENST00000690804.1:c.*525G>T ENSP00000508568.1:n.*525G>T
ENST00000692768.1:c.366G>T ENSP00000510254.1:p.Met122Ile
ENST00000693229.1:c.489G>T ENSP00000509223.1:p.Met163Ile
ENST00000256078.10:c.*118G>T MANE Plus Clinical ENSP00000256078.5:n.*118G>T
ENST00000311936.8:c.564G>T MANE Select ENSP00000308495.3:p.Met188Ile
ENST00000256078.8:c.*118G>T ENSP00000256078.4:n.*118G>T
ENST00000311936.7:c.564G>T ENSP00000308495.3:p.Met188Ile
ENST00000557334.5:c.225G>T ENSP00000452512.1:p.Met75Ile
NM_004985.4:c.564G>T NP_004976.2:p.Met188Ile
NM_033360.3:c.*118G>T NP_203524.1:n.*118G>T
XM_011520653.1:c.564G>T XP_011518955.1:p.Met188Ile
XM_011520653.3:c.564G>T XP_011518955.1:p.Met188Ile
NM_001369786.1:c.*118G>T NP_001356715.1:n.*118G>T
NM_001369787.1:c.564G>T NP_001356716.1:p.Met188Ile
NM_004985.5:c.564G>T MANE Select NP_004976.2:p.Met188Ile
NM_033360.4:c.*118G>T MANE Plus Clinical NP_203524.1:n.*118G>T