Canonical Allele Identifier: CA603691324
Gene: KRAS HGNC NCBI

Linked Data

dbSNP Id: rs1380921636

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209809_25209810del , CM000674.2:g.25209809_25209810del GRCh38
NC_000012.11:g.25362743_25362744del , CM000674.1:g.25362743_25362744del GRCh37
NC_000012.10:g.25254010_25254011del NCBI36
NG_007524.1:g.46115_46116del
NG_007524.2:g.46198_46199del

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.217_218del ENSP00000452512.1:p.Val73AsnfsTer25
ENST00000685328.1:c.556_557del ENSP00000508921.1:p.Val186AsnfsTer25
ENST00000686877.1:c.*527_*528del ENSP00000510431.1:n.*527_*528del
ENST00000687356.1:c.*254_*255del ENSP00000510511.1:n.*254_*255del
ENST00000688228.1:n.1030_1031del
ENST00000688940.1:c.556_557del ENSP00000509238.1:p.Val186AsnfsTer25
ENST00000690406.1:c.359_360del
ENST00000690804.1:c.*517_*518del ENSP00000508568.1:n.*517_*518del
ENST00000692768.1:c.358_359del ENSP00000510254.1:p.Val120AsnfsTer25
ENST00000693229.1:c.481_482del ENSP00000509223.1:p.Val161AsnfsTer25
ENST00000256078.10:c.*110_*111del MANE Plus Clinical ENSP00000256078.5:n.*110_*111del
ENST00000311936.8:c.556_557del MANE Select ENSP00000308495.3:p.Val186AsnfsTer25
ENST00000256078.8:c.*110_*111del ENSP00000256078.4:n.*110_*111del
ENST00000311936.7:c.556_557del ENSP00000308495.3:p.Val186AsnfsTer25
ENST00000557334.5:c.217_218del ENSP00000452512.1:p.Val73AsnfsTer25
NM_004985.4:c.556_557del NP_004976.2:p.Val186AsnfsTer25
NM_033360.3:c.*110_*111del NP_203524.1:n.*110_*111del
XM_011520653.1:c.556_557del XP_011518955.1:p.Val186AsnfsTer25
XM_011520653.3:c.556_557del XP_011518955.1:p.Val186AsnfsTer25
NM_001369786.1:c.*110_*111del NP_001356715.1:n.*110_*111del
NM_001369787.1:c.556_557del NP_001356716.1:p.Val186AsnfsTer25
NM_004985.5:c.556_557del MANE Select NP_004976.2:p.Val186AsnfsTer25
NM_033360.4:c.*110_*111del MANE Plus Clinical NP_203524.1:n.*110_*111del