Canonical Allele Identifier: CA2022884419
Gene: KRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209704G= , CM000674.2:g.25209704G= GRCh38
NC_000012.11:g.25362638G= , CM000674.1:g.25362638G= GRCh37
NC_000012.10:g.25253905G= NCBI36
NG_007524.1:g.46217C=
NG_007524.2:g.46300C=

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.*91C= ENSP00000452512.1:n.*91C=
ENST00000685328.1:c.*91C= ENSP00000508921.1:n.*91C=
ENST00000686877.1:c.*629C= ENSP00000510431.1:n.*629C=
ENST00000687356.1:c.*356C= ENSP00000510511.1:n.*356C=
ENST00000688228.1:n.1132C=
ENST00000688940.1:c.*91C= ENSP00000509238.1:n.*91C=
ENST00000690406.1:c.461C=
ENST00000690804.1:c.*619C= ENSP00000508568.1:n.*619C=
ENST00000692768.1:c.*91C= ENSP00000510254.1:n.*91C=
ENST00000693229.1:c.*91C= ENSP00000509223.1:n.*91C=
ENST00000256078.10:c.*212C= MANE Plus Clinical ENSP00000256078.5:n.*212C=
ENST00000311936.8:c.*91C= MANE Select ENSP00000308495.3:n.*91C=
ENST00000256078.8:c.*212C= ENSP00000256078.4:n.*212C=
ENST00000311936.7:c.*91C= ENSP00000308495.3:n.*91C=
ENST00000557334.5:c.*91C= ENSP00000452512.1:n.*91C=
NM_004985.4:c.*91C= NP_004976.2:n.*91C=
NM_033360.3:c.*212C= NP_203524.1:n.*212C=
XM_011520653.1:c.*91C= XP_011518955.1:n.*91C=
XM_011520653.3:c.*91C= XP_011518955.1:n.*91C=
NM_001369786.1:c.*212C= NP_001356715.1:n.*212C=
NM_001369787.1:c.*91C= NP_001356716.1:n.*91C=
NM_004985.5:c.*91C= MANE Select NP_004976.2:n.*91C=
NM_033360.4:c.*212C= MANE Plus Clinical NP_203524.1:n.*212C=