Canonical Allele Identifier: CA261707

Gene: KRAS

Linked Data

• ClinVar Variation Id: 40465
• ClinVar RCV Id: RCV000038274 ; RCV000157939 ; RCV000526276
• dbSNP Id: rs104894360
• gnomAD v4: 12-25209904-T-C
• MyVariant Identifiers: chr12:g.25362838T>C (hg19) ; chr12:g.25209904T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209904T>C , CM000674.2:g.25209904T>C	GRCh38
NC_000012.11:g.25362838T>C , CM000674.1:g.25362838T>C	GRCh37
NC_000012.10:g.25254105T>C	NCBI36
NG_007524.1:g.46017A>G
NG_007524.2:g.46100A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.119A>G	ENSP00000452512.1:p.Asp40Gly
ENST00000685328.1:c.458A>G	ENSP00000508921.1:p.Asp153Gly
ENST00000686877.1:c.*429A>G	ENSP00000510431.1:n.*429A>G
ENST00000687356.1:c.*156A>G	ENSP00000510511.1:n.*156A>G
ENST00000688228.1:n.932A>G
ENST00000688940.1:c.458A>G	ENSP00000509238.1:p.Asp153Gly
ENST00000690406.1:c.261A>G
ENST00000690804.1:c.*419A>G	ENSP00000508568.1:n.*419A>G
ENST00000692768.1:c.260A>G	ENSP00000510254.1:p.Asp87Gly
ENST00000693229.1:c.383A>G	ENSP00000509223.1:p.Asp128Gly
ENST00000256078.10:c.*12A>G MANE Plus Clinical	ENSP00000256078.5:n.*12A>G
ENST00000311936.8:c.458A>G MANE Select	ENSP00000308495.3:p.Asp153Gly
ENST00000256078.8:c.*12A>G	ENSP00000256078.4:n.*12A>G
ENST00000311936.7:c.458A>G	ENSP00000308495.3:p.Asp153Gly
ENST00000557334.5:c.119A>G	ENSP00000452512.1:p.Asp40Gly
NM_004985.4:c.458A>G	NP_004976.2:p.Asp153Gly
NM_033360.3:c.*12A>G	NP_203524.1:n.*12A>G
XM_006719069.2:c.*12A>G	XP_006719132.1:n.*12A>G
XM_011520653.1:c.458A>G	XP_011518955.1:p.Asp153Gly
XM_006719069.4:c.*12A>G	XP_006719132.1:n.*12A>G
XM_011520653.3:c.458A>G	XP_011518955.1:p.Asp153Gly
NM_001369786.1:c.*12A>G	NP_001356715.1:n.*12A>G
NM_001369787.1:c.458A>G	NP_001356716.1:p.Asp153Gly
NM_004985.5:c.458A>G MANE Select	NP_004976.2:p.Asp153Gly
NM_033360.4:c.*12A>G MANE Plus Clinical	NP_203524.1:n.*12A>G