Canonical Allele Identifier: CA2022905611

Gene: KRAS

Linked Data

• dbSNP Id: rs1951380875

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225477dup , CM000674.2:g.25225477dup	GRCh38
NC_000012.11:g.25378411dup , CM000674.1:g.25378411dup	GRCh37
NC_000012.10:g.25269678dup	NCBI36
NG_007524.1:g.30444dup
NG_007524.2:g.30527dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-15566dup	ENSP00000452512.1:n.112-15566dup
ENST00000685328.1:c.450+137dup	ENSP00000508921.1:n.450+137dup
ENST00000686877.1:c.*421+137dup	ENSP00000510431.1:n.*421+137dup
ENST00000687356.1:c.*148+137dup	ENSP00000510511.1:n.*148+137dup
ENST00000688228.1:n.924+137dup
ENST00000688940.1:c.450+137dup	ENSP00000509238.1:n.450+137dup
ENST00000690406.1:c.160+137dup
ENST00000690804.1:c.*411+137dup	ENSP00000508568.1:n.*411+137dup
ENST00000692768.1:c.252+137dup	ENSP00000510254.1:n.252+137dup
ENST00000693229.1:c.375+137dup	ENSP00000509223.1:n.375+137dup
ENST00000256078.10:c.450+137dup MANE Plus Clinical	ENSP00000256078.5:n.450+137dup
ENST00000311936.8:c.450+137dup MANE Select	ENSP00000308495.3:n.450+137dup
ENST00000256078.8:c.450+137dup	ENSP00000256078.4:n.450+137dup
ENST00000311936.7:c.450+137dup	ENSP00000308495.3:n.450+137dup
ENST00000557334.5:c.112-15566dup	ENSP00000452512.1:n.112-15566dup
NM_004985.4:c.450+137dup	NP_004976.2:n.450+137dup
NM_033360.3:c.450+137dup	NP_203524.1:n.450+137dup
XM_006719069.2:c.450+137dup	XP_006719132.1:n.450+137dup
XM_011520653.1:c.450+137dup	XP_011518955.1:n.450+137dup
XM_006719069.4:c.450+137dup	XP_006719132.1:n.450+137dup
XM_011520653.3:c.450+137dup	XP_011518955.1:n.450+137dup
NM_001369786.1:c.450+137dup	NP_001356715.1:n.450+137dup
NM_001369787.1:c.450+137dup	NP_001356716.1:n.450+137dup
NM_004985.5:c.450+137dup MANE Select	NP_004976.2:n.450+137dup
NM_033360.4:c.450+137dup MANE Plus Clinical	NP_203524.1:n.450+137dup