Canonical Allele Identifier: CA16602443
Gene: KRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 375966
dbSNP Id: rs121913240

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25227342T>G , CM000674.2:g.25227342T>G GRCh38
NC_000012.11:g.25380276T>G , CM000674.1:g.25380276T>G GRCh37
NC_000012.10:g.25271543T>G NCBI36
NG_007524.1:g.28579A>C
NG_007524.2:g.28662A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.112-17431A>C ENSP00000452512.1:n.112-17431A>C
ENST00000685328.1:c.182A>C ENSP00000508921.1:p.Gln61Pro
ENST00000686877.1:c.*153A>C ENSP00000510431.1:n.*153A>C
ENST00000687356.1:c.112-1569A>C ENSP00000510511.1:n.112-1569A>C
ENST00000688228.1:n.656A>C
ENST00000688940.1:c.182A>C ENSP00000509238.1:p.Gln61Pro
ENST00000690804.1:c.*143A>C ENSP00000508568.1:n.*143A>C
ENST00000692768.1:c.-17A>C ENSP00000510254.1:n.-17A>C
ENST00000693229.1:c.112-5A>C ENSP00000509223.1:n.112-5A>C
ENST00000256078.10:c.182A>C MANE Plus Clinical ENSP00000256078.5:p.Gln61Pro
ENST00000311936.8:c.182A>C MANE Select ENSP00000308495.3:p.Gln61Pro
ENST00000256078.8:c.182A>C ENSP00000256078.4:p.Gln61Pro
ENST00000311936.7:c.182A>C ENSP00000308495.3:p.Gln61Pro
ENST00000557334.5:c.112-17431A>C ENSP00000452512.1:n.112-17431A>C
NM_004985.4:c.182A>C NP_004976.2:p.Gln61Pro
NM_033360.3:c.182A>C NP_203524.1:p.Gln61Pro
XM_006719069.2:c.182A>C XP_006719132.1:p.Gln61Pro
XM_011520653.1:c.182A>C XP_011518955.1:p.Gln61Pro
XM_006719069.4:c.182A>C XP_006719132.1:p.Gln61Pro
XM_011520653.3:c.182A>C XP_011518955.1:p.Gln61Pro
NM_001369786.1:c.182A>C NP_001356715.1:p.Gln61Pro
NM_001369787.1:c.182A>C NP_001356716.1:p.Gln61Pro
NM_004985.5:c.182A>C MANE Select NP_004976.2:p.Gln61Pro
NM_033360.4:c.182A>C MANE Plus Clinical NP_203524.1:p.Gln61Pro