Canonical Allele Identifier: CA6486878
Gene: KRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2023985
ClinVar RCV Id: RCV002862980
dbSNP Id: rs766109434

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25225632T>C , CM000674.2:g.25225632T>C GRCh38
NC_000012.11:g.25378566T>C , CM000674.1:g.25378566T>C GRCh37
NC_000012.10:g.25269833T>C NCBI36
NG_007524.1:g.30289A>G
NG_007524.2:g.30372A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.112-15721A>G ENSP00000452512.1:n.112-15721A>G
ENST00000685328.1:c.432A>G ENSP00000508921.1:p.Thr144=
ENST00000686877.1:c.*403A>G ENSP00000510431.1:n.*403A>G
ENST00000687356.1:c.*130A>G ENSP00000510511.1:n.*130A>G
ENST00000688228.1:n.906A>G
ENST00000688940.1:c.432A>G ENSP00000509238.1:p.Thr144=
ENST00000690406.1:c.142A>G
ENST00000690804.1:c.*393A>G ENSP00000508568.1:n.*393A>G
ENST00000692768.1:c.234A>G ENSP00000510254.1:p.Thr78=
ENST00000693229.1:c.357A>G ENSP00000509223.1:p.Thr119=
ENST00000256078.10:c.432A>G MANE Plus Clinical ENSP00000256078.5:p.Thr144=
ENST00000311936.8:c.432A>G MANE Select ENSP00000308495.3:p.Thr144=
ENST00000256078.8:c.432A>G ENSP00000256078.4:p.Thr144=
ENST00000311936.7:c.432A>G ENSP00000308495.3:p.Thr144=
ENST00000557334.5:c.112-15721A>G ENSP00000452512.1:n.112-15721A>G
NM_004985.4:c.432A>G NP_004976.2:p.Thr144=
NM_033360.3:c.432A>G NP_203524.1:p.Thr144=
XM_006719069.2:c.432A>G XP_006719132.1:p.Thr144=
XM_011520653.1:c.432A>G XP_011518955.1:p.Thr144=
XM_006719069.4:c.432A>G XP_006719132.1:p.Thr144=
XM_011520653.3:c.432A>G XP_011518955.1:p.Thr144=
NM_001369786.1:c.432A>G NP_001356715.1:p.Thr144=
NM_001369787.1:c.432A>G NP_001356716.1:p.Thr144=
NM_004985.5:c.432A>G MANE Select NP_004976.2:p.Thr144=
NM_033360.4:c.432A>G MANE Plus Clinical NP_203524.1:p.Thr144=