Canonical Allele Identifier: CA384151222

Gene: KRAS

Linked Data

• dbSNP Id: rs1951383559
• COSMIC: COSM4040967 ; COSM4040968
• MyVariant Identifiers: chr12:g.25378594C>G (hg19) ; chr12:g.25225660C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225660C>G , CM000674.2:g.25225660C>G	GRCh38
NC_000012.11:g.25378594C>G , CM000674.1:g.25378594C>G	GRCh37
NC_000012.10:g.25269861C>G	NCBI36
NG_007524.1:g.30261G>C
NG_007524.2:g.30344G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15749G>C	ENSP00000452512.1:n.112-15749G>C
ENST00000685328.1:c.404G>C	ENSP00000508921.1:p.Arg135Thr
ENST00000686877.1:c.*375G>C	ENSP00000510431.1:n.*375G>C
ENST00000687356.1:c.*102G>C	ENSP00000510511.1:n.*102G>C
ENST00000688228.1:n.878G>C
ENST00000688940.1:c.404G>C	ENSP00000509238.1:p.Arg135Thr
ENST00000690406.1:c.114G>C
ENST00000690804.1:c.*365G>C	ENSP00000508568.1:n.*365G>C
ENST00000692768.1:c.206G>C	ENSP00000510254.1:p.Arg69Thr
ENST00000693229.1:c.329G>C	ENSP00000509223.1:p.Arg110Thr
ENST00000256078.10:c.404G>C MANE Plus Clinical	ENSP00000256078.5:p.Arg135Thr
ENST00000311936.8:c.404G>C MANE Select	ENSP00000308495.3:p.Arg135Thr
ENST00000256078.8:c.404G>C	ENSP00000256078.4:p.Arg135Thr
ENST00000311936.7:c.404G>C	ENSP00000308495.3:p.Arg135Thr
ENST00000557334.5:c.112-15749G>C	ENSP00000452512.1:n.112-15749G>C
NM_004985.4:c.404G>C	NP_004976.2:p.Arg135Thr
NM_033360.3:c.404G>C	NP_203524.1:p.Arg135Thr
XM_006719069.2:c.404G>C	XP_006719132.1:p.Arg135Thr
XM_011520653.1:c.404G>C	XP_011518955.1:p.Arg135Thr
XM_006719069.4:c.404G>C	XP_006719132.1:p.Arg135Thr
XM_011520653.3:c.404G>C	XP_011518955.1:p.Arg135Thr
NM_001369786.1:c.404G>C	NP_001356715.1:p.Arg135Thr
NM_001369787.1:c.404G>C	NP_001356716.1:p.Arg135Thr
NM_004985.5:c.404G>C MANE Select	NP_004976.2:p.Arg135Thr
NM_033360.4:c.404G>C MANE Plus Clinical	NP_203524.1:p.Arg135Thr