Canonical Allele Identifier: CA156358
Gene: KRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12589
dbSNP Id: rs104894365

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25245345C>T , CM000674.2:g.25245345C>T GRCh38
NC_000012.11:g.25398279C>T , CM000674.1:g.25398279C>T GRCh37
NC_000012.10:g.25289546C>T NCBI36
NG_007524.1:g.10576G>A
NG_007524.2:g.10659G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256078.10:c.40G>A ENSP00000256078.5:p.Val14Ile
ENST00000311936.8:c.40G>A MANE Select ENSP00000308495.3:p.Val14Ile
ENST00000256078.8:c.40G>A ENSP00000256078.4:p.Val14Ile
ENST00000311936.7:c.40G>A ENSP00000308495.3:p.Val14Ile
ENST00000556131.1:c.40G>A ENSP00000451856.1:p.Val14Ile
ENST00000557334.5:c.40G>A ENSP00000452512.1:p.Val14Ile
NM_004985.4:c.40G>A NP_004976.2:p.Val14Ile
NM_033360.3:c.40G>A NP_203524.1:p.Val14Ile
XM_006719069.2:c.40G>A XP_006719132.1:p.Val14Ile
XM_011520653.1:c.40G>A XP_011518955.1:p.Val14Ile
XM_006719069.4:c.40G>A XP_006719132.1:p.Val14Ile
XM_011520653.3:c.40G>A XP_011518955.1:p.Val14Ile
NM_001369786.1:c.40G>A NP_001356715.1:p.Val14Ile
NM_001369787.1:c.40G>A NP_001356716.1:p.Val14Ile
NM_004985.5:c.40G>A MANE Select NP_004976.2:p.Val14Ile
NM_033360.4:c.40G>A NP_203524.1:p.Val14Ile