Canonical Allele Identifier: CA384148481

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25362815G>C (hg19) ; chr12:g.25209881G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209881G>C , CM000674.2:g.25209881G>C	GRCh38
NC_000012.11:g.25362815G>C , CM000674.1:g.25362815G>C	GRCh37
NC_000012.10:g.25254082G>C	NCBI36
NG_007524.1:g.46040C>G
NG_007524.2:g.46123C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.142C>G	ENSP00000452512.1:p.Arg48Gly
ENST00000685328.1:c.481C>G	ENSP00000508921.1:p.Arg161Gly
ENST00000686877.1:c.*452C>G	ENSP00000510431.1:n.*452C>G
ENST00000687356.1:c.*179C>G	ENSP00000510511.1:n.*179C>G
ENST00000688228.1:n.955C>G
ENST00000688940.1:c.481C>G	ENSP00000509238.1:p.Arg161Gly
ENST00000690406.1:c.284C>G
ENST00000690804.1:c.*442C>G	ENSP00000508568.1:n.*442C>G
ENST00000692768.1:c.283C>G	ENSP00000510254.1:p.Arg95Gly
ENST00000693229.1:c.406C>G	ENSP00000509223.1:p.Arg136Gly
ENST00000256078.10:c.*35C>G MANE Plus Clinical	ENSP00000256078.5:n.*35C>G
ENST00000311936.8:c.481C>G MANE Select	ENSP00000308495.3:p.Arg161Gly
ENST00000256078.8:c.*35C>G	ENSP00000256078.4:n.*35C>G
ENST00000311936.7:c.481C>G	ENSP00000308495.3:p.Arg161Gly
ENST00000557334.5:c.142C>G	ENSP00000452512.1:p.Arg48Gly
NM_004985.4:c.481C>G	NP_004976.2:p.Arg161Gly
NM_033360.3:c.*35C>G	NP_203524.1:n.*35C>G
XM_006719069.2:c.*35C>G	XP_006719132.1:n.*35C>G
XM_011520653.1:c.481C>G	XP_011518955.1:p.Arg161Gly
XM_006719069.4:c.*35C>G	XP_006719132.1:n.*35C>G
XM_011520653.3:c.481C>G	XP_011518955.1:p.Arg161Gly
NM_001369786.1:c.*35C>G	NP_001356715.1:n.*35C>G
NM_001369787.1:c.481C>G	NP_001356716.1:p.Arg161Gly
NM_004985.5:c.481C>G MANE Select	NP_004976.2:p.Arg161Gly
NM_033360.4:c.*35C>G MANE Plus Clinical	NP_203524.1:n.*35C>G