Canonical Allele Identifier: CA384151382

Gene: KRAS

Linked Data

• dbSNP Id: rs1951384303
• MyVariant Identifiers: chr12:g.25378630C>A (hg19) ; chr12:g.25225696C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225696C>A , CM000674.2:g.25225696C>A	GRCh38
NC_000012.11:g.25378630C>A , CM000674.1:g.25378630C>A	GRCh37
NC_000012.10:g.25269897C>A	NCBI36
NG_007524.1:g.30225G>T
NG_007524.2:g.30308G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15785G>T	ENSP00000452512.1:n.112-15785G>T
ENST00000685328.1:c.368G>T	ENSP00000508921.1:p.Arg123Ile
ENST00000686877.1:c.*339G>T	ENSP00000510431.1:n.*339G>T
ENST00000687356.1:c.*66G>T	ENSP00000510511.1:n.*66G>T
ENST00000688228.1:n.842G>T
ENST00000688940.1:c.368G>T	ENSP00000509238.1:p.Arg123Ile
ENST00000690406.1:c.78G>T
ENST00000690804.1:c.*329G>T	ENSP00000508568.1:n.*329G>T
ENST00000692768.1:c.170G>T	ENSP00000510254.1:p.Arg57Ile
ENST00000693229.1:c.293G>T	ENSP00000509223.1:p.Arg98Ile
ENST00000256078.10:c.368G>T MANE Plus Clinical	ENSP00000256078.5:p.Arg123Ile
ENST00000311936.8:c.368G>T MANE Select	ENSP00000308495.3:p.Arg123Ile
ENST00000256078.8:c.368G>T	ENSP00000256078.4:p.Arg123Ile
ENST00000311936.7:c.368G>T	ENSP00000308495.3:p.Arg123Ile
ENST00000557334.5:c.112-15785G>T	ENSP00000452512.1:n.112-15785G>T
NM_004985.4:c.368G>T	NP_004976.2:p.Arg123Ile
NM_033360.3:c.368G>T	NP_203524.1:p.Arg123Ile
XM_006719069.2:c.368G>T	XP_006719132.1:p.Arg123Ile
XM_011520653.1:c.368G>T	XP_011518955.1:p.Arg123Ile
XM_006719069.4:c.368G>T	XP_006719132.1:p.Arg123Ile
XM_011520653.3:c.368G>T	XP_011518955.1:p.Arg123Ile
NM_001369786.1:c.368G>T	NP_001356715.1:p.Arg123Ile
NM_001369787.1:c.368G>T	NP_001356716.1:p.Arg123Ile
NM_004985.5:c.368G>T MANE Select	NP_004976.2:p.Arg123Ile
NM_033360.4:c.368G>T MANE Plus Clinical	NP_203524.1:p.Arg123Ile