Canonical Allele Identifier: CA2022884523
Gene: KRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209809_25209815delinsACTTTGT , CM000674.2:g.25209809_25209815delinsACTTTGT GRCh38
NC_000012.11:g.25362743_25362749delinsACTTTGT , CM000674.1:g.25362743_25362749delinsACTTTGT GRCh37
NC_000012.10:g.25254010_25254016delinsACTTTGT NCBI36
NG_007524.1:g.46106_46112delinsACAAAGT
NG_007524.2:g.46189_46195delinsACAAAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000557334.6:c.208_214delinsACAAAGT ENSP00000452512.1:p.Thr70=
ENST00000685328.1:c.547_553delinsACAAAGT ENSP00000508921.1:p.Thr183=
ENST00000686877.1:c.*518_*524delinsACAAAGT ENSP00000510431.1:n.*518_*524delinsACAAAGT
ENST00000687356.1:c.*245_*251delinsACAAAGT ENSP00000510511.1:n.*245_*251delinsACAAAGT
ENST00000688228.1:n.1021_1027delinsACAAAGT
ENST00000688940.1:c.547_553delinsACAAAGT ENSP00000509238.1:p.Thr183=
ENST00000690406.1:c.350_356delinsACAAAGT
ENST00000690804.1:c.*508_*514delinsACAAAGT ENSP00000508568.1:n.*508_*514delinsACAAAGT
ENST00000692768.1:c.349_355delinsACAAAGT ENSP00000510254.1:p.Thr117=
ENST00000693229.1:c.472_478delinsACAAAGT ENSP00000509223.1:p.Thr158=
ENST00000256078.10:c.*101_*107delinsACAAAGT MANE Plus Clinical ENSP00000256078.5:n.*101_*107delinsACAAAGT
ENST00000311936.8:c.547_553delinsACAAAGT MANE Select ENSP00000308495.3:p.Thr183=
ENST00000256078.8:c.*101_*107delinsACAAAGT ENSP00000256078.4:n.*101_*107delinsACAAAGT
ENST00000311936.7:c.547_553delinsACAAAGT ENSP00000308495.3:p.Thr183=
ENST00000557334.5:c.208_214delinsACAAAGT ENSP00000452512.1:p.Thr70=
NM_004985.4:c.547_553delinsACAAAGT NP_004976.2:p.Thr183=
NM_033360.3:c.*101_*107delinsACAAAGT NP_203524.1:n.*101_*107delinsACAAAGT
XM_011520653.1:c.547_553delinsACAAAGT XP_011518955.1:p.Thr183=
XM_011520653.3:c.547_553delinsACAAAGT XP_011518955.1:p.Thr183=
NM_001369786.1:c.*101_*107delinsACAAAGT NP_001356715.1:n.*101_*107delinsACAAAGT
NM_001369787.1:c.547_553delinsACAAAGT NP_001356716.1:p.Thr183=
NM_004985.5:c.547_553delinsACAAAGT MANE Select NP_004976.2:p.Thr183=
NM_033360.4:c.*101_*107delinsACAAAGT MANE Plus Clinical NP_203524.1:n.*101_*107delinsACAAAGT