Canonical Allele Identifier: CA185958

Gene: KRAS

Linked Data

• ClinVar Variation Id: 180715
• ClinVar RCV Id: RCV000157669
• dbSNP Id: rs730880380
• MyVariant Identifiers: chr12:g.25362813T>C (hg19) ; chr12:g.25209879T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209879T>C , CM000674.2:g.25209879T>C	GRCh38
NC_000012.11:g.25362813T>C , CM000674.1:g.25362813T>C	GRCh37
NC_000012.10:g.25254080T>C	NCBI36
NG_007524.1:g.46042A>G
NG_007524.2:g.46125A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.144A>G	ENSP00000452512.1:p.Arg48=
ENST00000685328.1:c.483A>G	ENSP00000508921.1:p.Arg161=
ENST00000686877.1:c.*454A>G	ENSP00000510431.1:n.*454A>G
ENST00000687356.1:c.*181A>G	ENSP00000510511.1:n.*181A>G
ENST00000688228.1:n.957A>G
ENST00000688940.1:c.483A>G	ENSP00000509238.1:p.Arg161=
ENST00000690406.1:c.286A>G
ENST00000690804.1:c.*444A>G	ENSP00000508568.1:n.*444A>G
ENST00000692768.1:c.285A>G	ENSP00000510254.1:p.Arg95=
ENST00000693229.1:c.408A>G	ENSP00000509223.1:p.Arg136=
ENST00000256078.10:c.*37A>G MANE Plus Clinical	ENSP00000256078.5:n.*37A>G
ENST00000311936.8:c.483A>G MANE Select	ENSP00000308495.3:p.Arg161=
ENST00000256078.8:c.*37A>G	ENSP00000256078.4:n.*37A>G
ENST00000311936.7:c.483A>G	ENSP00000308495.3:p.Arg161=
ENST00000557334.5:c.144A>G	ENSP00000452512.1:p.Arg48=
NM_004985.4:c.483A>G	NP_004976.2:p.Arg161=
NM_033360.3:c.*37A>G	NP_203524.1:n.*37A>G
XM_006719069.2:c.*37A>G	XP_006719132.1:n.*37A>G
XM_011520653.1:c.483A>G	XP_011518955.1:p.Arg161=
XM_006719069.4:c.*37A>G	XP_006719132.1:n.*37A>G
XM_011520653.3:c.483A>G	XP_011518955.1:p.Arg161=
NM_001369786.1:c.*37A>G	NP_001356715.1:n.*37A>G
NM_001369787.1:c.483A>G	NP_001356716.1:p.Arg161=
NM_004985.5:c.483A>G MANE Select	NP_004976.2:p.Arg161=
NM_033360.4:c.*37A>G MANE Plus Clinical	NP_203524.1:n.*37A>G