Canonical Allele Identifier: CA384151062
Gene: KRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25225624T>G , CM000674.2:g.25225624T>G GRCh38
NC_000012.11:g.25378558T>G , CM000674.1:g.25378558T>G GRCh37
NC_000012.10:g.25269825T>G NCBI36
NG_007524.1:g.30297A>C
NG_007524.2:g.30380A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256078.10:c.440A>C ENSP00000256078.5:p.Lys147Thr
ENST00000311936.8:c.440A>C MANE Select ENSP00000308495.3:p.Lys147Thr
ENST00000256078.8:c.440A>C ENSP00000256078.4:p.Lys147Thr
ENST00000311936.7:c.440A>C ENSP00000308495.3:p.Lys147Thr
ENST00000557334.5:c.112-15713A>C ENSP00000452512.1:p.=
NM_004985.4:c.440A>C NP_004976.2:p.Lys147Thr
NM_033360.3:c.440A>C NP_203524.1:p.Lys147Thr
XM_006719069.2:c.440A>C XP_006719132.1:p.Lys147Thr
XM_011520653.1:c.440A>C XP_011518955.1:p.Lys147Thr
XM_006719069.4:c.440A>C XP_006719132.1:p.Lys147Thr
XM_011520653.3:c.440A>C XP_011518955.1:p.Lys147Thr
NM_001369786.1:c.440A>C NP_001356715.1:p.Lys147Thr
NM_001369787.1:c.440A>C NP_001356716.1:p.Lys147Thr
NM_004985.5:c.440A>C MANE Select NP_004976.2:p.Lys147Thr
NM_033360.4:c.440A>C NP_203524.1:p.Lys147Thr