Canonical Allele Identifier: CA261709

Gene: KRAS

Linked Data

• ClinVar Variation Id: 45127
• ClinVar RCV Id: RCV000038275 ; RCV000157941
• dbSNP Id: rs397517042
• MyVariant Identifiers: chr12:g.25362830A>C (hg19) ; chr12:g.25209896A>C (hg38)
• PubMed: PMID:17056636 ; PMID:17601930

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209896A>C , CM000674.2:g.25209896A>C	GRCh38
NC_000012.11:g.25362830A>C , CM000674.1:g.25362830A>C	GRCh37
NC_000012.10:g.25254097A>C	NCBI36
NG_007524.1:g.46025T>G
NG_007524.2:g.46108T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.127T>G	ENSP00000452512.1:p.Phe43Val
ENST00000685328.1:c.466T>G	ENSP00000508921.1:p.Phe156Val
ENST00000686877.1:c.*437T>G	ENSP00000510431.1:n.*437T>G
ENST00000687356.1:c.*164T>G	ENSP00000510511.1:n.*164T>G
ENST00000688228.1:n.940T>G
ENST00000688940.1:c.466T>G	ENSP00000509238.1:p.Phe156Val
ENST00000690406.1:c.269T>G
ENST00000690804.1:c.*427T>G	ENSP00000508568.1:n.*427T>G
ENST00000692768.1:c.268T>G	ENSP00000510254.1:p.Phe90Val
ENST00000693229.1:c.391T>G	ENSP00000509223.1:p.Phe131Val
ENST00000256078.10:c.*20T>G MANE Plus Clinical	ENSP00000256078.5:n.*20T>G
ENST00000311936.8:c.466T>G MANE Select	ENSP00000308495.3:p.Phe156Val
ENST00000256078.8:c.*20T>G	ENSP00000256078.4:n.*20T>G
ENST00000311936.7:c.466T>G	ENSP00000308495.3:p.Phe156Val
ENST00000557334.5:c.127T>G	ENSP00000452512.1:p.Phe43Val
NM_004985.4:c.466T>G	NP_004976.2:p.Phe156Val
NM_033360.3:c.*20T>G	NP_203524.1:n.*20T>G
XM_006719069.2:c.*20T>G	XP_006719132.1:n.*20T>G
XM_011520653.1:c.466T>G	XP_011518955.1:p.Phe156Val
XM_006719069.4:c.*20T>G	XP_006719132.1:n.*20T>G
XM_011520653.3:c.466T>G	XP_011518955.1:p.Phe156Val
NM_001369786.1:c.*20T>G	NP_001356715.1:n.*20T>G
NM_001369787.1:c.466T>G	NP_001356716.1:p.Phe156Val
NM_004985.5:c.466T>G MANE Select	NP_004976.2:p.Phe156Val
NM_033360.4:c.*20T>G MANE Plus Clinical	NP_203524.1:n.*20T>G