Canonical Allele Identifier: CA2726042034

Gene: KRAS

Linked Data

• dbSNP Id: rs2141505736

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225650dup , CM000674.2:g.25225650dup	GRCh38
NC_000012.11:g.25378584dup , CM000674.1:g.25378584dup	GRCh37
NC_000012.10:g.25269851dup	NCBI36
NG_007524.1:g.30272dup
NG_007524.2:g.30355dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15738dup	ENSP00000452512.1:n.112-15738dup
ENST00000685328.1:c.415dup	ENSP00000508921.1:p.Ile139AsnfsTer5
ENST00000686877.1:c.*386dup	ENSP00000510431.1:n.*386dup
ENST00000687356.1:c.*113dup	ENSP00000510511.1:n.*113dup
ENST00000688228.1:n.889dup
ENST00000688940.1:c.415dup	ENSP00000509238.1:p.Ile139AsnfsTer5
ENST00000690406.1:c.125dup
ENST00000690804.1:c.*376dup	ENSP00000508568.1:n.*376dup
ENST00000692768.1:c.217dup	ENSP00000510254.1:p.Ile73AsnfsTer5
ENST00000693229.1:c.340dup	ENSP00000509223.1:p.Ile114AsnfsTer5
ENST00000256078.10:c.415dup MANE Plus Clinical	ENSP00000256078.5:p.Ile139AsnfsTer5
ENST00000311936.8:c.415dup MANE Select	ENSP00000308495.3:p.Ile139AsnfsTer5
ENST00000256078.8:c.415dup	ENSP00000256078.4:p.Ile139AsnfsTer5
ENST00000311936.7:c.415dup	ENSP00000308495.3:p.Ile139AsnfsTer5
ENST00000557334.5:c.112-15738dup	ENSP00000452512.1:n.112-15738dup
NM_004985.4:c.415dup	NP_004976.2:p.Ile139AsnfsTer5
NM_033360.3:c.415dup	NP_203524.1:p.Ile139AsnfsTer5
XM_006719069.2:c.415dup	XP_006719132.1:p.Ile139AsnfsTer5
XM_011520653.1:c.415dup	XP_011518955.1:p.Ile139AsnfsTer5
XM_006719069.4:c.415dup	XP_006719132.1:p.Ile139AsnfsTer5
XM_011520653.3:c.415dup	XP_011518955.1:p.Ile139AsnfsTer5
NM_001369786.1:c.415dup	NP_001356715.1:p.Ile139AsnfsTer5
NM_001369787.1:c.415dup	NP_001356716.1:p.Ile139AsnfsTer5
NM_004985.5:c.415dup MANE Select	NP_004976.2:p.Ile139AsnfsTer5
NM_033360.4:c.415dup MANE Plus Clinical	NP_203524.1:p.Ile139AsnfsTer5