Canonical Allele Identifier: CA384148530

Gene: KRAS

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209905C>T , CM000674.2:g.25209905C>T	GRCh38
NC_000012.11:g.25362839C>T , CM000674.1:g.25362839C>T	GRCh37
NC_000012.10:g.25254106C>T	NCBI36
NG_007524.1:g.46016G>A
NG_007524.2:g.46099G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.118G>A	ENSP00000452512.1:p.Asp40Asn
ENST00000685328.1:c.457G>A	ENSP00000508921.1:p.Asp153Asn
ENST00000686877.1:c.*428G>A	ENSP00000510431.1:n.*428G>A
ENST00000687356.1:c.*155G>A	ENSP00000510511.1:n.*155G>A
ENST00000688228.1:n.931G>A
ENST00000688940.1:c.457G>A	ENSP00000509238.1:p.Asp153Asn
ENST00000690406.1:c.260G>A
ENST00000690804.1:c.*418G>A	ENSP00000508568.1:n.*418G>A
ENST00000692768.1:c.259G>A	ENSP00000510254.1:p.Asp87Asn
ENST00000693229.1:c.382G>A	ENSP00000509223.1:p.Asp128Asn
ENST00000256078.10:c.*11G>A MANE Plus Clinical	ENSP00000256078.5:n.*11G>A
ENST00000311936.8:c.457G>A MANE Select	ENSP00000308495.3:p.Asp153Asn
ENST00000256078.8:c.*11G>A	ENSP00000256078.4:n.*11G>A
ENST00000311936.7:c.457G>A	ENSP00000308495.3:p.Asp153Asn
ENST00000557334.5:c.118G>A	ENSP00000452512.1:p.Asp40Asn
NM_004985.4:c.457G>A	NP_004976.2:p.Asp153Asn
NM_033360.3:c.*11G>A	NP_203524.1:n.*11G>A
XM_006719069.2:c.*11G>A	XP_006719132.1:n.*11G>A
XM_011520653.1:c.457G>A	XP_011518955.1:p.Asp153Asn
XM_006719069.4:c.*11G>A	XP_006719132.1:n.*11G>A
XM_011520653.3:c.457G>A	XP_011518955.1:p.Asp153Asn
NM_001369786.1:c.*11G>A	NP_001356715.1:n.*11G>A
NM_001369787.1:c.457G>A	NP_001356716.1:p.Asp153Asn
NM_004985.5:c.457G>A MANE Select	NP_004976.2:p.Asp153Asn
NM_033360.4:c.*11G>A MANE Plus Clinical	NP_203524.1:n.*11G>A