Canonical Allele Identifier: CA10641646

Linked Data

ClinVar Variation Id: 308071
dbSNP Id: rs188922523

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25206244G>C , CM000674.2:g.25206244G>C GRCh38
NC_000012.11:g.25359178G>C , CM000674.1:g.25359178G>C GRCh37
NC_000012.10:g.25250445G>C NCBI36
NG_007524.1:g.49677C>G
NG_007524.2:g.49760C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000685328.1:c.*3551C>G (KRAS) ENSP00000508921.1:n.*3551C>G
ENST00000686877.1:c.*4089C>G (KRAS) ENSP00000510431.1:n.*4089C>G
ENST00000687356.1:c.*3816C>G (KRAS) ENSP00000510511.1:n.*3816C>G
ENST00000690406.1:c.3921C>G (KRAS)
ENST00000692768.1:c.*3551C>G (KRAS) ENSP00000510254.1:n.*3551C>G
ENST00000693229.1:c.*3551C>G (KRAS) ENSP00000509223.1:n.*3551C>G
ENST00000256078.10:c.*3672C>G (KRAS) MANE Plus Clinical ENSP00000256078.5:n.*3672C>G
ENST00000311936.8:c.*3551C>G (KRAS) MANE Select ENSP00000308495.3:n.*3551C>G
ENST00000553788.6:c.51+2237G>C (ETFRF1) ENSP00000451938.2:n.51+2237G>C
ENST00000311936.7:c.*3551C>G (KRAS) ENSP00000308495.3:n.*3551C>G
ENST00000553788.5:c.45+2237G>C (ETFRF1) ENSP00000451938.1:n.45+2237G>C
NM_004985.4:c.*3551C>G (KRAS) NP_004976.2:n.*3551C>G
NM_033360.3:c.*3672C>G (KRAS) NP_203524.1:n.*3672C>G
XM_011520653.1:c.*3551C>G (KRAS) XP_011518955.1:n.*3551C>G
XM_011520653.3:c.*3551C>G (KRAS) XP_011518955.1:n.*3551C>G
NM_001369786.1:c.*3672C>G (KRAS) NP_001356715.1:n.*3672C>G
NM_001369787.1:c.*3551C>G (KRAS) NP_001356716.1:n.*3551C>G
NM_004985.5:c.*3551C>G (KRAS) MANE Select NP_004976.2:n.*3551C>G
NM_033360.4:c.*3672C>G (KRAS) MANE Plus Clinical NP_203524.1:n.*3672C>G