Canonical Allele Identifier: CA384148290

Gene: KRAS

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209802A>G , CM000674.2:g.25209802A>G	GRCh38
NC_000012.11:g.25362736A>G , CM000674.1:g.25362736A>G	GRCh37
NC_000012.10:g.25254003A>G	NCBI36
NG_007524.1:g.46119T>C
NG_007524.2:g.46202T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.221T>C	ENSP00000452512.1:p.Ile74Thr
ENST00000685328.1:c.560T>C	ENSP00000508921.1:p.Ile187Thr
ENST00000686877.1:c.*531T>C	ENSP00000510431.1:n.*531T>C
ENST00000687356.1:c.*258T>C	ENSP00000510511.1:n.*258T>C
ENST00000688228.1:n.1034T>C
ENST00000688940.1:c.560T>C	ENSP00000509238.1:p.Ile187Thr
ENST00000690406.1:c.363T>C
ENST00000690804.1:c.*521T>C	ENSP00000508568.1:n.*521T>C
ENST00000692768.1:c.362T>C	ENSP00000510254.1:p.Ile121Thr
ENST00000693229.1:c.485T>C	ENSP00000509223.1:p.Ile162Thr
ENST00000256078.10:c.*114T>C MANE Plus Clinical	ENSP00000256078.5:n.*114T>C
ENST00000311936.8:c.560T>C MANE Select	ENSP00000308495.3:p.Ile187Thr
ENST00000256078.8:c.*114T>C	ENSP00000256078.4:n.*114T>C
ENST00000311936.7:c.560T>C	ENSP00000308495.3:p.Ile187Thr
ENST00000557334.5:c.221T>C	ENSP00000452512.1:p.Ile74Thr
NM_004985.4:c.560T>C	NP_004976.2:p.Ile187Thr
NM_033360.3:c.*114T>C	NP_203524.1:n.*114T>C
XM_011520653.1:c.560T>C	XP_011518955.1:p.Ile187Thr
XM_011520653.3:c.560T>C	XP_011518955.1:p.Ile187Thr
NM_001369786.1:c.*114T>C	NP_001356715.1:n.*114T>C
NM_001369787.1:c.560T>C	NP_001356716.1:p.Ile187Thr
NM_004985.5:c.560T>C MANE Select	NP_004976.2:p.Ile187Thr
NM_033360.4:c.*114T>C MANE Plus Clinical	NP_203524.1:n.*114T>C