Canonical Allele Identifier: CA2022880943

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25206162_25206164delinsCTT , CM000674.2:g.25206162_25206164delinsCTT GRCh38
NC_000012.11:g.25359096_25359098delinsCTT , CM000674.1:g.25359096_25359098delinsCTT GRCh37
NC_000012.10:g.25250363_25250365delinsCTT NCBI36
NG_007524.1:g.49757_49759delinsAAG
NG_007524.2:g.49840_49842delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000685328.1:c.*3631_*3633delinsAAG (KRAS) ENSP00000508921.1:n.*3631_*3633delinsAAG
ENST00000686877.1:c.*4169_*4171delinsAAG (KRAS) ENSP00000510431.1:n.*4169_*4171delinsAAG
ENST00000687356.1:c.*3896_*3898delinsAAG (KRAS) ENSP00000510511.1:n.*3896_*3898delinsAAG
ENST00000690406.1:c.4001_4003delinsAAG (KRAS)
ENST00000692768.1:c.*3631_*3633delinsAAG (KRAS) ENSP00000510254.1:n.*3631_*3633delinsAAG
ENST00000693229.1:c.*3631_*3633delinsAAG (KRAS) ENSP00000509223.1:n.*3631_*3633delinsAAG
ENST00000256078.10:c.*3752_*3754delinsAAG (KRAS) MANE Plus Clinical ENSP00000256078.5:n.*3752_*3754delinsAAG
ENST00000311936.8:c.*3631_*3633delinsAAG (KRAS) MANE Select ENSP00000308495.3:n.*3631_*3633delinsAAG
ENST00000553788.6:c.51+2155_51+2157delinsCTT (ETFRF1) ENSP00000451938.2:n.51+2155_51+2157delinsCTT
ENST00000311936.7:c.*3631_*3633delinsAAG (KRAS) ENSP00000308495.3:n.*3631_*3633delinsAAG
ENST00000553788.5:c.45+2155_45+2157delinsCTT (ETFRF1) ENSP00000451938.1:n.45+2155_45+2157delinsCTT
NM_004985.4:c.*3631_*3633delinsAAG (KRAS) NP_004976.2:n.*3631_*3633delinsAAG
NM_033360.3:c.*3752_*3754delinsAAG (KRAS) NP_203524.1:n.*3752_*3754delinsAAG
XM_011520653.1:c.*3631_*3633delinsAAG (KRAS) XP_011518955.1:n.*3631_*3633delinsAAG
XM_011520653.3:c.*3631_*3633delinsAAG (KRAS) XP_011518955.1:n.*3631_*3633delinsAAG
NM_001369786.1:c.*3752_*3754delinsAAG (KRAS) NP_001356715.1:n.*3752_*3754delinsAAG
NM_001369787.1:c.*3631_*3633delinsAAG (KRAS) NP_001356716.1:n.*3631_*3633delinsAAG
NM_004985.5:c.*3631_*3633delinsAAG (KRAS) MANE Select NP_004976.2:n.*3631_*3633delinsAAG
NM_033360.4:c.*3752_*3754delinsAAG (KRAS) MANE Plus Clinical NP_203524.1:n.*3752_*3754delinsAAG