Canonical Allele Identifier: CA384151266
Gene: KRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25225670C>A , CM000674.2:g.25225670C>A GRCh38
NC_000012.11:g.25378604C>A , CM000674.1:g.25378604C>A GRCh37
NC_000012.10:g.25269871C>A NCBI36
NG_007524.1:g.30251G>T
NG_007524.2:g.30334G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000557334.6:c.112-15759G>T ENSP00000452512.1:n.112-15759G>T
ENST00000685328.1:c.394G>T ENSP00000508921.1:p.Asp132Tyr
ENST00000686877.1:c.*365G>T ENSP00000510431.1:n.*365G>T
ENST00000687356.1:c.*92G>T ENSP00000510511.1:n.*92G>T
ENST00000688228.1:n.868G>T
ENST00000688940.1:c.394G>T ENSP00000509238.1:p.Asp132Tyr
ENST00000690406.1:c.104G>T
ENST00000690804.1:c.*355G>T ENSP00000508568.1:n.*355G>T
ENST00000692768.1:c.196G>T ENSP00000510254.1:p.Asp66Tyr
ENST00000693229.1:c.319G>T ENSP00000509223.1:p.Asp107Tyr
ENST00000256078.10:c.394G>T MANE Plus Clinical ENSP00000256078.5:p.Asp132Tyr
ENST00000311936.8:c.394G>T MANE Select ENSP00000308495.3:p.Asp132Tyr
ENST00000256078.8:c.394G>T ENSP00000256078.4:p.Asp132Tyr
ENST00000311936.7:c.394G>T ENSP00000308495.3:p.Asp132Tyr
ENST00000557334.5:c.112-15759G>T ENSP00000452512.1:n.112-15759G>T
NM_004985.4:c.394G>T NP_004976.2:p.Asp132Tyr
NM_033360.3:c.394G>T NP_203524.1:p.Asp132Tyr
XM_006719069.2:c.394G>T XP_006719132.1:p.Asp132Tyr
XM_011520653.1:c.394G>T XP_011518955.1:p.Asp132Tyr
XM_006719069.4:c.394G>T XP_006719132.1:p.Asp132Tyr
XM_011520653.3:c.394G>T XP_011518955.1:p.Asp132Tyr
NM_001369786.1:c.394G>T NP_001356715.1:p.Asp132Tyr
NM_001369787.1:c.394G>T NP_001356716.1:p.Asp132Tyr
NM_004985.5:c.394G>T MANE Select NP_004976.2:p.Asp132Tyr
NM_033360.4:c.394G>T MANE Plus Clinical NP_203524.1:p.Asp132Tyr