Canonical Allele Identifier: CA384151294
Gene: KRAS HGNC NCBI

Linked Data

dbSNP Id: rs1463850736

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25225676C>T , CM000674.2:g.25225676C>T GRCh38
NC_000012.11:g.25378610C>T , CM000674.1:g.25378610C>T GRCh37
NC_000012.10:g.25269877C>T NCBI36
NG_007524.1:g.30245G>A
NG_007524.2:g.30328G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000557334.6:c.112-15765G>A ENSP00000452512.1:n.112-15765G>A
ENST00000685328.1:c.388G>A ENSP00000508921.1:p.Ala130Thr
ENST00000686877.1:c.*359G>A ENSP00000510431.1:n.*359G>A
ENST00000687356.1:c.*86G>A ENSP00000510511.1:n.*86G>A
ENST00000688228.1:n.862G>A
ENST00000688940.1:c.388G>A ENSP00000509238.1:p.Ala130Thr
ENST00000690406.1:c.98G>A
ENST00000690804.1:c.*349G>A ENSP00000508568.1:n.*349G>A
ENST00000692768.1:c.190G>A ENSP00000510254.1:p.Ala64Thr
ENST00000693229.1:c.313G>A ENSP00000509223.1:p.Ala105Thr
ENST00000256078.10:c.388G>A MANE Plus Clinical ENSP00000256078.5:p.Ala130Thr
ENST00000311936.8:c.388G>A MANE Select ENSP00000308495.3:p.Ala130Thr
ENST00000256078.8:c.388G>A ENSP00000256078.4:p.Ala130Thr
ENST00000311936.7:c.388G>A ENSP00000308495.3:p.Ala130Thr
ENST00000557334.5:c.112-15765G>A ENSP00000452512.1:n.112-15765G>A
NM_004985.4:c.388G>A NP_004976.2:p.Ala130Thr
NM_033360.3:c.388G>A NP_203524.1:p.Ala130Thr
XM_006719069.2:c.388G>A XP_006719132.1:p.Ala130Thr
XM_011520653.1:c.388G>A XP_011518955.1:p.Ala130Thr
XM_006719069.4:c.388G>A XP_006719132.1:p.Ala130Thr
XM_011520653.3:c.388G>A XP_011518955.1:p.Ala130Thr
NM_001369786.1:c.388G>A NP_001356715.1:p.Ala130Thr
NM_001369787.1:c.388G>A NP_001356716.1:p.Ala130Thr
NM_004985.5:c.388G>A MANE Select NP_004976.2:p.Ala130Thr
NM_033360.4:c.388G>A MANE Plus Clinical NP_203524.1:p.Ala130Thr