Canonical Allele Identifier: CA2022884380
Gene: KRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209655G= , CM000674.2:g.25209655G= GRCh38
NC_000012.11:g.25362589G= , CM000674.1:g.25362589G= GRCh37
NC_000012.10:g.25253856G= NCBI36
NG_007524.1:g.46266C=
NG_007524.2:g.46349C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557334.6:c.*140C= ENSP00000452512.1:n.*140C=
ENST00000685328.1:c.*140C= ENSP00000508921.1:n.*140C=
ENST00000686877.1:c.*678C= ENSP00000510431.1:n.*678C=
ENST00000687356.1:c.*405C= ENSP00000510511.1:n.*405C=
ENST00000688940.1:c.*140C= ENSP00000509238.1:n.*140C=
ENST00000690406.1:c.510C=
ENST00000690804.1:c.*668C= ENSP00000508568.1:n.*668C=
ENST00000692768.1:c.*140C= ENSP00000510254.1:n.*140C=
ENST00000693229.1:c.*140C= ENSP00000509223.1:n.*140C=
ENST00000256078.10:c.*261C= MANE Plus Clinical ENSP00000256078.5:n.*261C=
ENST00000311936.8:c.*140C= MANE Select ENSP00000308495.3:n.*140C=
ENST00000256078.8:c.*261C= ENSP00000256078.4:n.*261C=
ENST00000311936.7:c.*140C= ENSP00000308495.3:n.*140C=
ENST00000557334.5:c.*140C= ENSP00000452512.1:n.*140C=
NM_004985.4:c.*140C= NP_004976.2:n.*140C=
NM_033360.3:c.*261C= NP_203524.1:n.*261C=
XM_011520653.1:c.*140C= XP_011518955.1:n.*140C=
XM_011520653.3:c.*140C= XP_011518955.1:n.*140C=
NM_001369786.1:c.*261C= NP_001356715.1:n.*261C=
NM_001369787.1:c.*140C= NP_001356716.1:n.*140C=
NM_004985.5:c.*140C= MANE Select NP_004976.2:n.*140C=
NM_033360.4:c.*261C= MANE Plus Clinical NP_203524.1:n.*261C=