Canonical Allele Identifier: CA384151145

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25378577A>C (hg19) ; chr12:g.25225643A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225643A>C , CM000674.2:g.25225643A>C	GRCh38
NC_000012.11:g.25378577A>C , CM000674.1:g.25378577A>C	GRCh37
NC_000012.10:g.25269844A>C	NCBI36
NG_007524.1:g.30278T>G
NG_007524.2:g.30361T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15732T>G	ENSP00000452512.1:n.112-15732T>G
ENST00000685328.1:c.421T>G	ENSP00000508921.1:p.Phe141Val
ENST00000686877.1:c.*392T>G	ENSP00000510431.1:n.*392T>G
ENST00000687356.1:c.*119T>G	ENSP00000510511.1:n.*119T>G
ENST00000688228.1:n.895T>G
ENST00000688940.1:c.421T>G	ENSP00000509238.1:p.Phe141Val
ENST00000690406.1:c.131T>G
ENST00000690804.1:c.*382T>G	ENSP00000508568.1:n.*382T>G
ENST00000692768.1:c.223T>G	ENSP00000510254.1:p.Phe75Val
ENST00000693229.1:c.346T>G	ENSP00000509223.1:p.Phe116Val
ENST00000256078.10:c.421T>G MANE Plus Clinical	ENSP00000256078.5:p.Phe141Val
ENST00000311936.8:c.421T>G MANE Select	ENSP00000308495.3:p.Phe141Val
ENST00000256078.8:c.421T>G	ENSP00000256078.4:p.Phe141Val
ENST00000311936.7:c.421T>G	ENSP00000308495.3:p.Phe141Val
ENST00000557334.5:c.112-15732T>G	ENSP00000452512.1:n.112-15732T>G
NM_004985.4:c.421T>G	NP_004976.2:p.Phe141Val
NM_033360.3:c.421T>G	NP_203524.1:p.Phe141Val
XM_006719069.2:c.421T>G	XP_006719132.1:p.Phe141Val
XM_011520653.1:c.421T>G	XP_011518955.1:p.Phe141Val
XM_006719069.4:c.421T>G	XP_006719132.1:p.Phe141Val
XM_011520653.3:c.421T>G	XP_011518955.1:p.Phe141Val
NM_001369786.1:c.421T>G	NP_001356715.1:p.Phe141Val
NM_001369787.1:c.421T>G	NP_001356716.1:p.Phe141Val
NM_004985.5:c.421T>G MANE Select	NP_004976.2:p.Phe141Val
NM_033360.4:c.421T>G MANE Plus Clinical	NP_203524.1:p.Phe141Val