Canonical Allele Identifier: CA919045445
Gene: KRAS HGNC NCBI

Linked Data

dbSNP Id: rs1592798700

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25215561_25215562del , CM000674.2:g.25215561_25215562del GRCh38
NC_000012.11:g.25368495_25368496del , CM000674.1:g.25368495_25368496del GRCh37
NC_000012.10:g.25259762_25259763del NCBI36
NG_007524.1:g.40363_40364del
NG_007524.2:g.40446_40447del

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.112-5647_112-5646del ENSP00000452512.1:n.112-5647_112-5646del
ENST00000685328.1:c.451-5647_451-5646del ENSP00000508921.1:n.451-5647_451-5646del
ENST00000686877.1:c.*422-5647_*422-5646del ENSP00000510431.1:n.*422-5647_*422-5646de...
ENST00000687356.1:c.*149-5647_*149-5646del ENSP00000510511.1:n.*149-5647_*149-5646de...
ENST00000688228.1:n.925-5647_925-5646del
ENST00000688940.1:c.451-5647_451-5646del ENSP00000509238.1:n.451-5647_451-5646del
ENST00000690406.1:c.161-2352_161-2351del
ENST00000690804.1:c.*412-5647_*412-5646del ENSP00000508568.1:n.*412-5647_*412-5646de...
ENST00000692768.1:c.253-5647_253-5646del ENSP00000510254.1:n.253-5647_253-5646del
ENST00000693229.1:c.376-5647_376-5646del ENSP00000509223.1:n.376-5647_376-5646del
ENST00000256078.10:c.453_454del
ENST00000311936.8:c.451-5647_451-5646del MANE Select ENSP00000308495.3:n.451-5647_451-5646del
ENST00000256078.8:c.453_454del
ENST00000311936.7:c.451-5647_451-5646del ENSP00000308495.3:n.451-5647_451-5646del
ENST00000557334.5:c.112-5647_112-5646del ENSP00000452512.1:n.112-5647_112-5646del
NM_004985.4:c.451-5647_451-5646del NP_004976.2:n.451-5647_451-5646del
NM_033360.3:c.453_454del
XM_006719069.2:c.453_454del
XM_011520653.1:c.451-5647_451-5646del XP_011518955.1:n.451-5647_451-5646del
XM_006719069.4:c.453_454del
XM_011520653.3:c.451-5647_451-5646del XP_011518955.1:n.451-5647_451-5646del
NM_001369786.1:c.453_454del
NM_001369787.1:c.451-5647_451-5646del NP_001356716.1:n.451-5647_451-5646del
NM_004985.5:c.451-5647_451-5646del MANE Select NP_004976.2:n.451-5647_451-5646del
NM_033360.4:c.453_454del