Canonical Allele Identifier: CA384151509

Gene: KRAS

Linked Data

• dbSNP Id: rs2141506296
• gnomAD v4: 12-25225724-C-T
• COSMIC: COSM6474356 ; COSM6474357
• MyVariant Identifiers: chr12:g.25378658C>T (hg19) ; chr12:g.25225724C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225724C>T , CM000674.2:g.25225724C>T	GRCh38
NC_000012.11:g.25378658C>T , CM000674.1:g.25378658C>T	GRCh37
NC_000012.10:g.25269925C>T	NCBI36
NG_007524.1:g.30197G>A
NG_007524.2:g.30280G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15813G>A	ENSP00000452512.1:n.112-15813G>A
ENST00000685328.1:c.340G>A	ENSP00000508921.1:p.Val114Ile
ENST00000686877.1:c.*311G>A	ENSP00000510431.1:n.*311G>A
ENST00000687356.1:c.*38G>A	ENSP00000510511.1:n.*38G>A
ENST00000688228.1:n.814G>A
ENST00000688940.1:c.340G>A	ENSP00000509238.1:p.Val114Ile
ENST00000690406.1:c.50G>A
ENST00000690804.1:c.*301G>A	ENSP00000508568.1:n.*301G>A
ENST00000692768.1:c.142G>A	ENSP00000510254.1:p.Val48Ile
ENST00000693229.1:c.265G>A	ENSP00000509223.1:p.Val89Ile
ENST00000256078.10:c.340G>A MANE Plus Clinical	ENSP00000256078.5:p.Val114Ile
ENST00000311936.8:c.340G>A MANE Select	ENSP00000308495.3:p.Val114Ile
ENST00000256078.8:c.340G>A	ENSP00000256078.4:p.Val114Ile
ENST00000311936.7:c.340G>A	ENSP00000308495.3:p.Val114Ile
ENST00000557334.5:c.112-15813G>A	ENSP00000452512.1:n.112-15813G>A
NM_004985.4:c.340G>A	NP_004976.2:p.Val114Ile
NM_033360.3:c.340G>A	NP_203524.1:p.Val114Ile
XM_006719069.2:c.340G>A	XP_006719132.1:p.Val114Ile
XM_011520653.1:c.340G>A	XP_011518955.1:p.Val114Ile
XM_006719069.4:c.340G>A	XP_006719132.1:p.Val114Ile
XM_011520653.3:c.340G>A	XP_011518955.1:p.Val114Ile
NM_001369786.1:c.340G>A	NP_001356715.1:p.Val114Ile
NM_001369787.1:c.340G>A	NP_001356716.1:p.Val114Ile
NM_004985.5:c.340G>A MANE Select	NP_004976.2:p.Val114Ile
NM_033360.4:c.340G>A MANE Plus Clinical	NP_203524.1:p.Val114Ile