Canonical Allele Identifier: CA2575103909

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25227262del , CM000674.2:g.25227262del	GRCh38
NC_000012.11:g.25380196del , CM000674.1:g.25380196del	GRCh37
NC_000012.10:g.25271463del	NCBI36
NG_007524.1:g.28661del
NG_007524.2:g.28744del

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-17349del	ENSP00000452512.1:n.112-17349del
ENST00000685328.1:c.264del	ENSP00000508921.1:p.Lys88AsnfsTer26
ENST00000686877.1:c.*235del	ENSP00000510431.1:n.*235del
ENST00000687356.1:c.112-1487del	ENSP00000510511.1:n.112-1487del
ENST00000688228.1:n.738del
ENST00000688940.1:c.264del	ENSP00000509238.1:p.Lys88AsnfsTer26
ENST00000690804.1:c.*225del	ENSP00000508568.1:n.*225del
ENST00000692768.1:c.66del	ENSP00000510254.1:p.Lys22AsnfsTer26
ENST00000693229.1:c.189del	ENSP00000509223.1:p.Lys63AsnfsTer26
ENST00000256078.10:c.264del MANE Plus Clinical	ENSP00000256078.5:p.Lys88AsnfsTer26
ENST00000311936.8:c.264del MANE Select	ENSP00000308495.3:p.Lys88AsnfsTer26
ENST00000256078.8:c.264del	ENSP00000256078.4:p.Lys88AsnfsTer26
ENST00000311936.7:c.264del	ENSP00000308495.3:p.Lys88AsnfsTer26
ENST00000557334.5:c.112-17349del	ENSP00000452512.1:n.112-17349del
NM_004985.4:c.264del	NP_004976.2:p.Lys88AsnfsTer26
NM_033360.3:c.264del	NP_203524.1:p.Lys88AsnfsTer26
XM_006719069.2:c.264del	XP_006719132.1:p.Lys88AsnfsTer26
XM_011520653.1:c.264del	XP_011518955.1:p.Lys88AsnfsTer26
XM_006719069.4:c.264del	XP_006719132.1:p.Lys88AsnfsTer26
XM_011520653.3:c.264del	XP_011518955.1:p.Lys88AsnfsTer26
NM_001369786.1:c.264del	NP_001356715.1:p.Lys88AsnfsTer26
NM_001369787.1:c.264del	NP_001356716.1:p.Lys88AsnfsTer26
NM_004985.5:c.264del MANE Select	NP_004976.2:p.Lys88AsnfsTer26
NM_033360.4:c.264del MANE Plus Clinical	NP_203524.1:p.Lys88AsnfsTer26