Canonical Allele Identifier: CA2022881280

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25206530_25206531delinsTA , CM000674.2:g.25206530_25206531delinsTA GRCh38
NC_000012.11:g.25359464_25359465delinsTA , CM000674.1:g.25359464_25359465delinsTA GRCh37
NC_000012.10:g.25250731_25250732delinsTA NCBI36
NG_007524.1:g.49390_49391delinsTA
NG_007524.2:g.49473_49474delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000685328.1:c.*3264_*3265delinsTA (KRAS) ENSP00000508921.1:n.*3264_*3265delinsTA
ENST00000686877.1:c.*3802_*3803delinsTA (KRAS) ENSP00000510431.1:n.*3802_*3803delinsTA
ENST00000687356.1:c.*3529_*3530delinsTA (KRAS) ENSP00000510511.1:n.*3529_*3530delinsTA
ENST00000690406.1:c.3634_3635delinsTA (KRAS)
ENST00000692768.1:c.*3264_*3265delinsTA (KRAS) ENSP00000510254.1:n.*3264_*3265delinsTA
ENST00000693229.1:c.*3264_*3265delinsTA (KRAS) ENSP00000509223.1:n.*3264_*3265delinsTA
ENST00000256078.10:c.*3385_*3386delinsTA (KRAS) MANE Plus Clinical ENSP00000256078.5:n.*3385_*3386delinsTA
ENST00000311936.8:c.*3264_*3265delinsTA (KRAS) MANE Select ENSP00000308495.3:n.*3264_*3265delinsTA
ENST00000553788.6:c.51+2523_51+2524delinsTA (ETFRF1) ENSP00000451938.2:n.51+2523_51+2524delinsTA
ENST00000311936.7:c.*3264_*3265delinsTA (KRAS) ENSP00000308495.3:n.*3264_*3265delinsTA
ENST00000553788.5:c.45+2523_45+2524delinsTA (ETFRF1) ENSP00000451938.1:n.45+2523_45+2524delinsTA
NM_004985.4:c.*3264_*3265delinsTA (KRAS) NP_004976.2:n.*3264_*3265delinsTA
NM_033360.3:c.*3385_*3386delinsTA (KRAS) NP_203524.1:n.*3385_*3386delinsTA
XM_011520653.1:c.*3264_*3265delinsTA (KRAS) XP_011518955.1:n.*3264_*3265delinsTA
XM_011520653.3:c.*3264_*3265delinsTA (KRAS) XP_011518955.1:n.*3264_*3265delinsTA
NM_001369786.1:c.*3385_*3386delinsTA (KRAS) NP_001356715.1:n.*3385_*3386delinsTA
NM_001369787.1:c.*3264_*3265delinsTA (KRAS) NP_001356716.1:n.*3264_*3265delinsTA
NM_004985.5:c.*3264_*3265delinsTA (KRAS) MANE Select NP_004976.2:n.*3264_*3265delinsTA
NM_033360.4:c.*3385_*3386delinsTA (KRAS) MANE Plus Clinical NP_203524.1:n.*3385_*3386delinsTA