Canonical Allele Identifier: CA384148292
Gene: KRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209803T>A , CM000674.2:g.25209803T>A GRCh38
NC_000012.11:g.25362737T>A , CM000674.1:g.25362737T>A GRCh37
NC_000012.10:g.25254004T>A NCBI36
NG_007524.1:g.46118A>T
NG_007524.2:g.46201A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.220A>T ENSP00000452512.1:p.Ile74Phe
ENST00000685328.1:c.559A>T ENSP00000508921.1:p.Ile187Phe
ENST00000686877.1:c.*530A>T ENSP00000510431.1:n.*530A>T
ENST00000687356.1:c.*257A>T ENSP00000510511.1:n.*257A>T
ENST00000688228.1:n.1033A>T
ENST00000688940.1:c.559A>T ENSP00000509238.1:p.Ile187Phe
ENST00000690406.1:c.362A>T
ENST00000690804.1:c.*520A>T ENSP00000508568.1:n.*520A>T
ENST00000692768.1:c.361A>T ENSP00000510254.1:p.Ile121Phe
ENST00000693229.1:c.484A>T ENSP00000509223.1:p.Ile162Phe
ENST00000256078.10:c.*113A>T MANE Plus Clinical ENSP00000256078.5:n.*113A>T
ENST00000311936.8:c.559A>T MANE Select ENSP00000308495.3:p.Ile187Phe
ENST00000256078.8:c.*113A>T ENSP00000256078.4:n.*113A>T
ENST00000311936.7:c.559A>T ENSP00000308495.3:p.Ile187Phe
ENST00000557334.5:c.220A>T ENSP00000452512.1:p.Ile74Phe
NM_004985.4:c.559A>T NP_004976.2:p.Ile187Phe
NM_033360.3:c.*113A>T NP_203524.1:n.*113A>T
XM_011520653.1:c.559A>T XP_011518955.1:p.Ile187Phe
XM_011520653.3:c.559A>T XP_011518955.1:p.Ile187Phe
NM_001369786.1:c.*113A>T NP_001356715.1:n.*113A>T
NM_001369787.1:c.559A>T NP_001356716.1:p.Ile187Phe
NM_004985.5:c.559A>T MANE Select NP_004976.2:p.Ile187Phe
NM_033360.4:c.*113A>T MANE Plus Clinical NP_203524.1:n.*113A>T