Canonical Allele Identifier: CA645572097
Gene: KRAS HGNC NCBI

Linked Data

dbSNP Id: rs2141510086

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25227341_25227342delinsAC , CM000674.2:g.25227341_25227342delinsAC GRCh38
NC_000012.11:g.25380275_25380276delinsAC , CM000674.1:g.25380275_25380276delinsAC GRCh37
NC_000012.10:g.25271542_25271543delinsAC NCBI36
NG_007524.1:g.28579_28580delinsGT
NG_007524.2:g.28662_28663delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000557334.6:c.112-17431_112-17430delinsGT ENSP00000452512.1:n.112-17431_112-17430delinsGT
ENST00000685328.1:c.182_183delinsGT ENSP00000508921.1:p.Gln61Arg
ENST00000686877.1:c.*153_*154delinsGT ENSP00000510431.1:n.*153_*154delinsGT
ENST00000687356.1:c.112-1569_112-1568delinsGT ENSP00000510511.1:n.112-1569_112-1568delinsGT
ENST00000688228.1:n.656_657delinsGT
ENST00000688940.1:c.182_183delinsGT ENSP00000509238.1:p.Gln61Arg
ENST00000690804.1:c.*143_*144delinsGT ENSP00000508568.1:n.*143_*144delinsGT
ENST00000692768.1:c.-17_-16delinsGT ENSP00000510254.1:n.-17_-16delinsGT
ENST00000693229.1:c.112-5_112-4delinsGT ENSP00000509223.1:n.112-5_112-4delinsGT
ENST00000256078.10:c.182_183delinsGT MANE Plus Clinical ENSP00000256078.5:p.Gln61Arg
ENST00000311936.8:c.182_183delinsGT MANE Select ENSP00000308495.3:p.Gln61Arg
ENST00000256078.8:c.182_183delinsGT ENSP00000256078.4:p.Gln61Arg
ENST00000311936.7:c.182_183delinsGT ENSP00000308495.3:p.Gln61Arg
ENST00000557334.5:c.112-17431_112-17430delinsGT ENSP00000452512.1:n.112-17431_112-17430delinsGT
NM_004985.4:c.182_183delinsGT NP_004976.2:p.Gln61Arg
NM_033360.3:c.182_183delinsGT NP_203524.1:p.Gln61Arg
XM_006719069.2:c.182_183delinsGT XP_006719132.1:p.Gln61Arg
XM_011520653.1:c.182_183delinsGT XP_011518955.1:p.Gln61Arg
XM_006719069.4:c.182_183delinsGT XP_006719132.1:p.Gln61Arg
XM_011520653.3:c.182_183delinsGT XP_011518955.1:p.Gln61Arg
NM_001369786.1:c.182_183delinsGT NP_001356715.1:p.Gln61Arg
NM_001369787.1:c.182_183delinsGT NP_001356716.1:p.Gln61Arg
NM_004985.5:c.182_183delinsGT MANE Select NP_004976.2:p.Gln61Arg
NM_033360.4:c.182_183delinsGT MANE Plus Clinical NP_203524.1:p.Gln61Arg