Canonical Allele Identifier: CA279964
Gene: KRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12595
dbSNP Id: rs104894362

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209894G>C , CM000674.2:g.25209894G>C GRCh38
NC_000012.11:g.25362828G>C , CM000674.1:g.25362828G>C GRCh37
NC_000012.10:g.25254095G>C NCBI36
NG_007524.1:g.46027C>G
NG_007524.2:g.46110C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000256078.10:c.*22C>G ENSP00000256078.5:p.=
ENST00000311936.8:c.468C>G MANE Select ENSP00000308495.3:p.Phe156Leu
ENST00000256078.8:c.*22C>G ENSP00000256078.4:p.=
ENST00000311936.7:c.468C>G ENSP00000308495.3:p.Phe156Leu
ENST00000557334.5:c.129C>G ENSP00000452512.1:p.Phe43Leu
NM_004985.4:c.468C>G NP_004976.2:p.Phe156Leu
NM_033360.3:c.*22C>G NP_203524.1:p.=
XM_006719069.2:c.*22C>G XP_006719132.1:p.=
XM_011520653.1:c.468C>G XP_011518955.1:p.Phe156Leu
XM_006719069.4:c.*22C>G XP_006719132.1:p.=
XM_011520653.3:c.468C>G XP_011518955.1:p.Phe156Leu
NM_001369786.1:c.*22C>G NP_001356715.1:p.=
NM_001369787.1:c.468C>G NP_001356716.1:p.Phe156Leu
NM_004985.5:c.468C>G MANE Select NP_004976.2:p.Phe156Leu
NM_033360.4:c.*22C>G NP_203524.1:p.=