Canonical Allele Identifier: CA234206964

Gene: KRAS

Linked Data

• dbSNP Id: rs757674707
• gnomAD v4: 12-25209884-C-T
• MyVariant Identifiers: chr12:g.25362818C>T (hg19) ; chr12:g.25209884C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209884C>T , CM000674.2:g.25209884C>T	GRCh38
NC_000012.11:g.25362818C>T , CM000674.1:g.25362818C>T	GRCh37
NC_000012.10:g.25254085C>T	NCBI36
NG_007524.1:g.46037G>A
NG_007524.2:g.46120G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.139G>A	ENSP00000452512.1:p.Val47Ile
ENST00000685328.1:c.478G>A	ENSP00000508921.1:p.Val160Ile
ENST00000686877.1:c.*449G>A	ENSP00000510431.1:n.*449G>A
ENST00000687356.1:c.*176G>A	ENSP00000510511.1:n.*176G>A
ENST00000688228.1:n.952G>A
ENST00000688940.1:c.478G>A	ENSP00000509238.1:p.Val160Ile
ENST00000690406.1:c.281G>A
ENST00000690804.1:c.*439G>A	ENSP00000508568.1:n.*439G>A
ENST00000692768.1:c.280G>A	ENSP00000510254.1:p.Val94Ile
ENST00000693229.1:c.403G>A	ENSP00000509223.1:p.Val135Ile
ENST00000256078.10:c.*32G>A MANE Plus Clinical	ENSP00000256078.5:n.*32G>A
ENST00000311936.8:c.478G>A MANE Select	ENSP00000308495.3:p.Val160Ile
ENST00000256078.8:c.*32G>A	ENSP00000256078.4:n.*32G>A
ENST00000311936.7:c.478G>A	ENSP00000308495.3:p.Val160Ile
ENST00000557334.5:c.139G>A	ENSP00000452512.1:p.Val47Ile
NM_004985.4:c.478G>A	NP_004976.2:p.Val160Ile
NM_033360.3:c.*32G>A	NP_203524.1:n.*32G>A
XM_006719069.2:c.*32G>A	XP_006719132.1:n.*32G>A
XM_011520653.1:c.478G>A	XP_011518955.1:p.Val160Ile
XM_006719069.4:c.*32G>A	XP_006719132.1:n.*32G>A
XM_011520653.3:c.478G>A	XP_011518955.1:p.Val160Ile
NM_001369786.1:c.*32G>A	NP_001356715.1:n.*32G>A
NM_001369787.1:c.478G>A	NP_001356716.1:p.Val160Ile
NM_004985.5:c.478G>A MANE Select	NP_004976.2:p.Val160Ile
NM_033360.4:c.*32G>A MANE Plus Clinical	NP_203524.1:n.*32G>A