Canonical Allele Identifier: CA384151149

Gene: KRAS

Linked Data

• dbSNP Id: rs2141505704
• MyVariant Identifiers: chr12:g.25378577A>T (hg19) ; chr12:g.25225643A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15732T>A	ENSP00000452512.1:n.112-15732T>A
ENST00000685328.1:c.421T>A	ENSP00000508921.1:p.Phe141Ile
ENST00000686877.1:c.*392T>A	ENSP00000510431.1:n.*392T>A
ENST00000687356.1:c.*119T>A	ENSP00000510511.1:n.*119T>A
ENST00000688228.1:n.895T>A
ENST00000688940.1:c.421T>A	ENSP00000509238.1:p.Phe141Ile
ENST00000690406.1:c.131T>A
ENST00000690804.1:c.*382T>A	ENSP00000508568.1:n.*382T>A
ENST00000692768.1:c.223T>A	ENSP00000510254.1:p.Phe75Ile
ENST00000693229.1:c.346T>A	ENSP00000509223.1:p.Phe116Ile
ENST00000256078.10:c.421T>A MANE Plus Clinical	ENSP00000256078.5:p.Phe141Ile
ENST00000311936.8:c.421T>A MANE Select	ENSP00000308495.3:p.Phe141Ile
ENST00000256078.8:c.421T>A	ENSP00000256078.4:p.Phe141Ile
ENST00000311936.7:c.421T>A	ENSP00000308495.3:p.Phe141Ile
ENST00000557334.5:c.112-15732T>A	ENSP00000452512.1:n.112-15732T>A
NM_004985.4:c.421T>A	NP_004976.2:p.Phe141Ile
NM_033360.3:c.421T>A	NP_203524.1:p.Phe141Ile
XM_006719069.2:c.421T>A	XP_006719132.1:p.Phe141Ile
XM_011520653.1:c.421T>A	XP_011518955.1:p.Phe141Ile
XM_006719069.4:c.421T>A	XP_006719132.1:p.Phe141Ile
XM_011520653.3:c.421T>A	XP_011518955.1:p.Phe141Ile
NM_001369786.1:c.421T>A	NP_001356715.1:p.Phe141Ile
NM_001369787.1:c.421T>A	NP_001356716.1:p.Phe141Ile
NM_004985.5:c.421T>A MANE Select	NP_004976.2:p.Phe141Ile
NM_033360.4:c.421T>A MANE Plus Clinical	NP_203524.1:p.Phe141Ile