Canonical Allele Identifier: CA2022880791

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25206055_25206056delinsTA , CM000674.2:g.25206055_25206056delinsTA GRCh38
NC_000012.11:g.25358989_25358990delinsTA , CM000674.1:g.25358989_25358990delinsTA GRCh37
NC_000012.10:g.25250256_25250257delinsTA NCBI36
NG_007524.1:g.49865_49866delinsTA
NG_007524.2:g.49948_49949delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000685328.1:c.*3739_*3740delinsTA (KRAS) ENSP00000508921.1:n.*3739_*3740delinsTA
ENST00000686877.1:c.*4277_*4278delinsTA (KRAS) ENSP00000510431.1:n.*4277_*4278delinsTA
ENST00000687356.1:c.*4004_*4005delinsTA (KRAS) ENSP00000510511.1:n.*4004_*4005delinsTA
ENST00000690406.1:c.4109_4110delinsTA (KRAS)
ENST00000692768.1:c.*3739_*3740delinsTA (KRAS) ENSP00000510254.1:n.*3739_*3740delinsTA
ENST00000693229.1:c.*3739_*3740delinsTA (KRAS) ENSP00000509223.1:n.*3739_*3740delinsTA
ENST00000256078.10:c.*3860_*3861delinsTA (KRAS) MANE Plus Clinical ENSP00000256078.5:n.*3860_*3861delinsTA
ENST00000311936.8:c.*3739_*3740delinsTA (KRAS) MANE Select ENSP00000308495.3:n.*3739_*3740delinsTA
ENST00000553788.6:c.51+2048_51+2049delinsTA (ETFRF1) ENSP00000451938.2:n.51+2048_51+2049delins...
ENST00000311936.7:c.*3739_*3740delinsTA (KRAS) ENSP00000308495.3:n.*3739_*3740delinsTA
ENST00000553788.5:c.45+2048_45+2049delinsTA (ETFRF1) ENSP00000451938.1:n.45+2048_45+2049delins...
NM_004985.4:c.*3739_*3740delinsTA (KRAS) NP_004976.2:n.*3739_*3740delinsTA
NM_033360.3:c.*3860_*3861delinsTA (KRAS) NP_203524.1:n.*3860_*3861delinsTA
XM_011520653.1:c.*3739_*3740delinsTA (KRAS) XP_011518955.1:n.*3739_*3740delinsTA
XM_011520653.3:c.*3739_*3740delinsTA (KRAS) XP_011518955.1:n.*3739_*3740delinsTA
NM_001369786.1:c.*3860_*3861delinsTA (KRAS) NP_001356715.1:n.*3860_*3861delinsTA
NM_001369787.1:c.*3739_*3740delinsTA (KRAS) NP_001356716.1:n.*3739_*3740delinsTA
NM_004985.5:c.*3739_*3740delinsTA (KRAS) MANE Select NP_004976.2:n.*3739_*3740delinsTA
NM_033360.4:c.*3860_*3861delinsTA (KRAS) MANE Plus Clinical NP_203524.1:n.*3860_*3861delinsTA