Canonical Allele Identifier: CA384148293
Gene: KRAS HGNC NCBI

Linked Data

dbSNP Id: rs1233599652

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.220A>G ENSP00000452512.1:p.Ile74Val
ENST00000685328.1:c.559A>G ENSP00000508921.1:p.Ile187Val
ENST00000686877.1:c.*530A>G ENSP00000510431.1:n.*530A>G
ENST00000687356.1:c.*257A>G ENSP00000510511.1:n.*257A>G
ENST00000688228.1:n.1033A>G
ENST00000688940.1:c.559A>G ENSP00000509238.1:p.Ile187Val
ENST00000690406.1:c.362A>G
ENST00000690804.1:c.*520A>G ENSP00000508568.1:n.*520A>G
ENST00000692768.1:c.361A>G ENSP00000510254.1:p.Ile121Val
ENST00000693229.1:c.484A>G ENSP00000509223.1:p.Ile162Val
ENST00000256078.10:c.*113A>G MANE Plus Clinical ENSP00000256078.5:n.*113A>G
ENST00000311936.8:c.559A>G MANE Select ENSP00000308495.3:p.Ile187Val
ENST00000256078.8:c.*113A>G ENSP00000256078.4:n.*113A>G
ENST00000311936.7:c.559A>G ENSP00000308495.3:p.Ile187Val
ENST00000557334.5:c.220A>G ENSP00000452512.1:p.Ile74Val
NM_004985.4:c.559A>G NP_004976.2:p.Ile187Val
NM_033360.3:c.*113A>G NP_203524.1:n.*113A>G
XM_011520653.1:c.559A>G XP_011518955.1:p.Ile187Val
XM_011520653.3:c.559A>G XP_011518955.1:p.Ile187Val
NM_001369786.1:c.*113A>G NP_001356715.1:n.*113A>G
NM_001369787.1:c.559A>G NP_001356716.1:p.Ile187Val
NM_004985.5:c.559A>G MANE Select NP_004976.2:p.Ile187Val
NM_033360.4:c.*113A>G MANE Plus Clinical NP_203524.1:n.*113A>G