Canonical Allele Identifier: CA384148285
Gene: KRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209800T>A , CM000674.2:g.25209800T>A GRCh38
NC_000012.11:g.25362734T>A , CM000674.1:g.25362734T>A GRCh37
NC_000012.10:g.25254001T>A NCBI36
NG_007524.1:g.46121A>T
NG_007524.2:g.46204A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.223A>T ENSP00000452512.1:p.Met75Leu
ENST00000685328.1:c.562A>T ENSP00000508921.1:p.Met188Leu
ENST00000686877.1:c.*533A>T ENSP00000510431.1:n.*533A>T
ENST00000687356.1:c.*260A>T ENSP00000510511.1:n.*260A>T
ENST00000688228.1:n.1036A>T
ENST00000688940.1:c.562A>T ENSP00000509238.1:p.Met188Leu
ENST00000690406.1:c.365A>T
ENST00000690804.1:c.*523A>T ENSP00000508568.1:n.*523A>T
ENST00000692768.1:c.364A>T ENSP00000510254.1:p.Met122Leu
ENST00000693229.1:c.487A>T ENSP00000509223.1:p.Met163Leu
ENST00000256078.10:c.*116A>T MANE Plus Clinical ENSP00000256078.5:n.*116A>T
ENST00000311936.8:c.562A>T MANE Select ENSP00000308495.3:p.Met188Leu
ENST00000256078.8:c.*116A>T ENSP00000256078.4:n.*116A>T
ENST00000311936.7:c.562A>T ENSP00000308495.3:p.Met188Leu
ENST00000557334.5:c.223A>T ENSP00000452512.1:p.Met75Leu
NM_004985.4:c.562A>T NP_004976.2:p.Met188Leu
NM_033360.3:c.*116A>T NP_203524.1:n.*116A>T
XM_011520653.1:c.562A>T XP_011518955.1:p.Met188Leu
XM_011520653.3:c.562A>T XP_011518955.1:p.Met188Leu
NM_001369786.1:c.*116A>T NP_001356715.1:n.*116A>T
NM_001369787.1:c.562A>T NP_001356716.1:p.Met188Leu
NM_004985.5:c.562A>T MANE Select NP_004976.2:p.Met188Leu
NM_033360.4:c.*116A>T MANE Plus Clinical NP_203524.1:n.*116A>T