Canonical Allele Identifier: CA2575103830

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209853_25209855del , CM000674.2:g.25209853_25209855del	GRCh38
NC_000012.11:g.25362787_25362789del , CM000674.1:g.25362787_25362789del	GRCh37
NC_000012.10:g.25254054_25254056del	NCBI36
NG_007524.1:g.46068_46070del
NG_007524.2:g.46151_46153del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.170_172del	ENSP00000452512.1:p.Met57del
ENST00000685328.1:c.509_511del	ENSP00000508921.1:p.Met170del
ENST00000686877.1:c.*480_*482del	ENSP00000510431.1:n.*480_*482del
ENST00000687356.1:c.*207_*209del	ENSP00000510511.1:n.*207_*209del
ENST00000688228.1:n.983_985del
ENST00000688940.1:c.509_511del	ENSP00000509238.1:p.Met170del
ENST00000690406.1:c.312_314del
ENST00000690804.1:c.*470_*472del	ENSP00000508568.1:n.*470_*472del
ENST00000692768.1:c.311_313del	ENSP00000510254.1:p.Met104del
ENST00000693229.1:c.434_436del	ENSP00000509223.1:p.Met145del
ENST00000256078.10:c.*63_*65del MANE Plus Clinical	ENSP00000256078.5:n.*63_*65del
ENST00000311936.8:c.509_511del MANE Select	ENSP00000308495.3:p.Met170del
ENST00000256078.8:c.*63_*65del	ENSP00000256078.4:n.*63_*65del
ENST00000311936.7:c.509_511del	ENSP00000308495.3:p.Met170del
ENST00000557334.5:c.170_172del	ENSP00000452512.1:p.Met57del
NM_004985.4:c.509_511del	NP_004976.2:p.Met170del
NM_033360.3:c.*63_*65del	NP_203524.1:n.*63_*65del
XM_006719069.2:c.*63_*65del	XP_006719132.1:n.*63_*65del
XM_011520653.1:c.509_511del	XP_011518955.1:p.Met170del
XM_006719069.4:c.*63_*65del	XP_006719132.1:n.*63_*65del
XM_011520653.3:c.509_511del	XP_011518955.1:p.Met170del
NM_001369786.1:c.*63_*65del	NP_001356715.1:n.*63_*65del
NM_001369787.1:c.509_511del	NP_001356716.1:p.Met170del
NM_004985.5:c.509_511del MANE Select	NP_004976.2:p.Met170del
NM_033360.4:c.*63_*65del MANE Plus Clinical	NP_203524.1:n.*63_*65del