Canonical Allele Identifier: CA384148276

Gene: KRAS

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209797A>C , CM000674.2:g.25209797A>C	GRCh38
NC_000012.11:g.25362731A>C , CM000674.1:g.25362731A>C	GRCh37
NC_000012.10:g.25253998A>C	NCBI36
NG_007524.1:g.46124T>G
NG_007524.2:g.46207T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.226T>G	ENSP00000452512.1:p.Ter76Glu
ENST00000685328.1:c.565T>G	ENSP00000508921.1:p.Ter189Glu
ENST00000686877.1:c.*536T>G	ENSP00000510431.1:n.*536T>G
ENST00000687356.1:c.*263T>G	ENSP00000510511.1:n.*263T>G
ENST00000688228.1:n.1039T>G
ENST00000688940.1:c.565T>G	ENSP00000509238.1:p.Ter189Glu
ENST00000690406.1:c.368T>G
ENST00000690804.1:c.*526T>G	ENSP00000508568.1:n.*526T>G
ENST00000692768.1:c.367T>G	ENSP00000510254.1:p.Ter123Glu
ENST00000693229.1:c.490T>G	ENSP00000509223.1:p.Ter164Glu
ENST00000256078.10:c.*119T>G MANE Plus Clinical	ENSP00000256078.5:n.*119T>G
ENST00000311936.8:c.565T>G MANE Select	ENSP00000308495.3:p.Ter189Glu
ENST00000256078.8:c.*119T>G	ENSP00000256078.4:n.*119T>G
ENST00000311936.7:c.565T>G	ENSP00000308495.3:p.Ter189Glu
ENST00000557334.5:c.226T>G	ENSP00000452512.1:p.Ter76Glu
NM_004985.4:c.565T>G	NP_004976.2:p.Ter189Glu
NM_033360.3:c.*119T>G	NP_203524.1:n.*119T>G
XM_011520653.1:c.565T>G	XP_011518955.1:p.Ter189Glu
XM_011520653.3:c.565T>G	XP_011518955.1:p.Ter189Glu
NM_001369786.1:c.*119T>G	NP_001356715.1:n.*119T>G
NM_001369787.1:c.565T>G	NP_001356716.1:p.Ter189Glu
NM_004985.5:c.565T>G MANE Select	NP_004976.2:p.Ter189Glu
NM_033360.4:c.*119T>G MANE Plus Clinical	NP_203524.1:n.*119T>G