Canonical Allele Identifier: CA2022884452
Gene: KRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209743C= , CM000674.2:g.25209743C= GRCh38
NC_000012.11:g.25362677C= , CM000674.1:g.25362677C= GRCh37
NC_000012.10:g.25253944C= NCBI36
NG_007524.1:g.46178G=
NG_007524.2:g.46261G=

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.*52G= ENSP00000452512.1:n.*52G=
ENST00000685328.1:c.*52G= ENSP00000508921.1:n.*52G=
ENST00000686877.1:c.*590G= ENSP00000510431.1:n.*590G=
ENST00000687356.1:c.*317G= ENSP00000510511.1:n.*317G=
ENST00000688228.1:n.1093G=
ENST00000688940.1:c.*52G= ENSP00000509238.1:n.*52G=
ENST00000690406.1:c.422G=
ENST00000690804.1:c.*580G= ENSP00000508568.1:n.*580G=
ENST00000692768.1:c.*52G= ENSP00000510254.1:n.*52G=
ENST00000693229.1:c.*52G= ENSP00000509223.1:n.*52G=
ENST00000256078.10:c.*173G= MANE Plus Clinical ENSP00000256078.5:n.*173G=
ENST00000311936.8:c.*52G= MANE Select ENSP00000308495.3:n.*52G=
ENST00000256078.8:c.*173G= ENSP00000256078.4:n.*173G=
ENST00000311936.7:c.*52G= ENSP00000308495.3:n.*52G=
ENST00000557334.5:c.*52G= ENSP00000452512.1:n.*52G=
NM_004985.4:c.*52G= NP_004976.2:n.*52G=
NM_033360.3:c.*173G= NP_203524.1:n.*173G=
XM_011520653.1:c.*52G= XP_011518955.1:n.*52G=
XM_011520653.3:c.*52G= XP_011518955.1:n.*52G=
NM_001369786.1:c.*173G= NP_001356715.1:n.*173G=
NM_001369787.1:c.*52G= NP_001356716.1:n.*52G=
NM_004985.5:c.*52G= MANE Select NP_004976.2:n.*52G=
NM_033360.4:c.*173G= MANE Plus Clinical NP_203524.1:n.*173G=