Canonical Allele Identifier: CA384151152

Gene: KRAS

Linked Data

• dbSNP Id: rs2141505721
• MyVariant Identifiers: chr12:g.25378579G>C (hg19) ; chr12:g.25225645G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225645G>C , CM000674.2:g.25225645G>C	GRCh38
NC_000012.11:g.25378579G>C , CM000674.1:g.25378579G>C	GRCh37
NC_000012.10:g.25269846G>C	NCBI36
NG_007524.1:g.30276C>G
NG_007524.2:g.30359C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15734C>G	ENSP00000452512.1:n.112-15734C>G
ENST00000685328.1:c.419C>G	ENSP00000508921.1:p.Pro140Arg
ENST00000686877.1:c.*390C>G	ENSP00000510431.1:n.*390C>G
ENST00000687356.1:c.*117C>G	ENSP00000510511.1:n.*117C>G
ENST00000688228.1:n.893C>G
ENST00000688940.1:c.419C>G	ENSP00000509238.1:p.Pro140Arg
ENST00000690406.1:c.129C>G
ENST00000690804.1:c.*380C>G	ENSP00000508568.1:n.*380C>G
ENST00000692768.1:c.221C>G	ENSP00000510254.1:p.Pro74Arg
ENST00000693229.1:c.344C>G	ENSP00000509223.1:p.Pro115Arg
ENST00000256078.10:c.419C>G MANE Plus Clinical	ENSP00000256078.5:p.Pro140Arg
ENST00000311936.8:c.419C>G MANE Select	ENSP00000308495.3:p.Pro140Arg
ENST00000256078.8:c.419C>G	ENSP00000256078.4:p.Pro140Arg
ENST00000311936.7:c.419C>G	ENSP00000308495.3:p.Pro140Arg
ENST00000557334.5:c.112-15734C>G	ENSP00000452512.1:n.112-15734C>G
NM_004985.4:c.419C>G	NP_004976.2:p.Pro140Arg
NM_033360.3:c.419C>G	NP_203524.1:p.Pro140Arg
XM_006719069.2:c.419C>G	XP_006719132.1:p.Pro140Arg
XM_011520653.1:c.419C>G	XP_011518955.1:p.Pro140Arg
XM_006719069.4:c.419C>G	XP_006719132.1:p.Pro140Arg
XM_011520653.3:c.419C>G	XP_011518955.1:p.Pro140Arg
NM_001369786.1:c.419C>G	NP_001356715.1:p.Pro140Arg
NM_001369787.1:c.419C>G	NP_001356716.1:p.Pro140Arg
NM_004985.5:c.419C>G MANE Select	NP_004976.2:p.Pro140Arg
NM_033360.4:c.419C>G MANE Plus Clinical	NP_203524.1:p.Pro140Arg