Canonical Allele Identifier: CA2022889914
Gene: KRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25215281_25215282delinsTA , CM000674.2:g.25215281_25215282delinsTA GRCh38
NC_000012.11:g.25368215_25368216delinsTA , CM000674.1:g.25368215_25368216delinsTA GRCh37
NC_000012.10:g.25259482_25259483delinsTA NCBI36
NG_007524.1:g.40639_40640delinsTA
NG_007524.2:g.40722_40723delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.112-5371_112-5370delinsTA ENSP00000452512.1:n.112-5371_112-5370delinsTA
ENST00000685328.1:c.451-5371_451-5370delinsTA ENSP00000508921.1:n.451-5371_451-5370delinsTA
ENST00000686877.1:c.*422-5371_*422-5370delinsTA ENSP00000510431.1:n.*422-5371_*422-5370delinsTA
ENST00000687356.1:c.*149-5371_*149-5370delinsTA ENSP00000510511.1:n.*149-5371_*149-5370delinsTA
ENST00000688228.1:n.925-5371_925-5370delinsTA
ENST00000688940.1:c.451-5371_451-5370delinsTA ENSP00000509238.1:n.451-5371_451-5370delinsTA
ENST00000690406.1:c.161-2076_161-2075delinsTA
ENST00000690804.1:c.*412-5371_*412-5370delinsTA ENSP00000508568.1:n.*412-5371_*412-5370delinsTA
ENST00000692768.1:c.253-5371_253-5370delinsTA ENSP00000510254.1:n.253-5371_253-5370delinsTA
ENST00000693229.1:c.376-5371_376-5370delinsTA ENSP00000509223.1:n.376-5371_376-5370delinsTA
ENST00000256078.10:c.*4+155_*4+156delinsTA MANE Plus Clinical ENSP00000256078.5:n.*4+155_*4+156delinsTA
ENST00000311936.8:c.451-5371_451-5370delinsTA MANE Select ENSP00000308495.3:n.451-5371_451-5370delinsTA
ENST00000256078.8:c.*4+155_*4+156delinsTA ENSP00000256078.4:n.*4+155_*4+156delinsTA
ENST00000311936.7:c.451-5371_451-5370delinsTA ENSP00000308495.3:n.451-5371_451-5370delinsTA
ENST00000557334.5:c.112-5371_112-5370delinsTA ENSP00000452512.1:n.112-5371_112-5370delinsTA
NM_004985.4:c.451-5371_451-5370delinsTA NP_004976.2:n.451-5371_451-5370delinsTA
NM_033360.3:c.*4+155_*4+156delinsTA NP_203524.1:n.*4+155_*4+156delinsTA
XM_006719069.2:c.*4+155_*4+156delinsTA XP_006719132.1:n.*4+155_*4+156delinsTA
XM_011520653.1:c.451-5371_451-5370delinsTA XP_011518955.1:n.451-5371_451-5370delinsTA
XM_006719069.4:c.*4+155_*4+156delinsTA XP_006719132.1:n.*4+155_*4+156delinsTA
XM_011520653.3:c.451-5371_451-5370delinsTA XP_011518955.1:n.451-5371_451-5370delinsTA
NM_001369786.1:c.*4+155_*4+156delinsTA NP_001356715.1:n.*4+155_*4+156delinsTA
NM_001369787.1:c.451-5371_451-5370delinsTA NP_001356716.1:n.451-5371_451-5370delinsTA
NM_004985.5:c.451-5371_451-5370delinsTA MANE Select NP_004976.2:n.451-5371_451-5370delinsTA
NM_033360.4:c.*4+155_*4+156delinsTA MANE Plus Clinical NP_203524.1:n.*4+155_*4+156delinsTA