Canonical Allele Identifier: CA135580

Gene: KRAS

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209871C>T , CM000674.2:g.25209871C>T	GRCh38
NC_000012.11:g.25362805C>T , CM000674.1:g.25362805C>T	GRCh37
NC_000012.10:g.25254072C>T	NCBI36
NG_007524.1:g.46050G>A
NG_007524.2:g.46133G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.152G>A	ENSP00000452512.1:p.Arg51Gln
ENST00000685328.1:c.491G>A	ENSP00000508921.1:p.Arg164Gln
ENST00000686877.1:c.*462G>A	ENSP00000510431.1:n.*462G>A
ENST00000687356.1:c.*189G>A	ENSP00000510511.1:n.*189G>A
ENST00000688228.1:n.965G>A
ENST00000688940.1:c.491G>A	ENSP00000509238.1:p.Arg164Gln
ENST00000690406.1:c.294G>A
ENST00000690804.1:c.*452G>A	ENSP00000508568.1:n.*452G>A
ENST00000692768.1:c.293G>A	ENSP00000510254.1:p.Arg98Gln
ENST00000693229.1:c.416G>A	ENSP00000509223.1:p.Arg139Gln
ENST00000256078.10:c.*45G>A MANE Plus Clinical	ENSP00000256078.5:n.*45G>A
ENST00000311936.8:c.491G>A MANE Select	ENSP00000308495.3:p.Arg164Gln
ENST00000256078.8:c.*45G>A	ENSP00000256078.4:n.*45G>A
ENST00000311936.7:c.491G>A	ENSP00000308495.3:p.Arg164Gln
ENST00000557334.5:c.152G>A	ENSP00000452512.1:p.Arg51Gln
NM_004985.4:c.491G>A	NP_004976.2:p.Arg164Gln
NM_033360.3:c.*45G>A	NP_203524.1:n.*45G>A
XM_006719069.2:c.*45G>A	XP_006719132.1:n.*45G>A
XM_011520653.1:c.491G>A	XP_011518955.1:p.Arg164Gln
XM_006719069.4:c.*45G>A	XP_006719132.1:n.*45G>A
XM_011520653.3:c.491G>A	XP_011518955.1:p.Arg164Gln
NM_001369786.1:c.*45G>A	NP_001356715.1:n.*45G>A
NM_001369787.1:c.491G>A	NP_001356716.1:p.Arg164Gln
NM_004985.5:c.491G>A MANE Select	NP_004976.2:p.Arg164Gln
NM_033360.4:c.*45G>A MANE Plus Clinical	NP_203524.1:n.*45G>A