Canonical Allele Identifier: CA2794888677

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209570A>C , CM000674.2:g.25209570A>C GRCh38
NC_000012.11:g.25362504A>C , CM000674.1:g.25362504A>C GRCh37
NC_000012.10:g.25253771A>C NCBI36
NG_007524.1:g.46351T>G
NG_007524.2:g.46434T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000557334.6:c.*225T>G (KRAS) ENSP00000452512.1:n.*225T>G
ENST00000685328.1:c.*225T>G (KRAS) ENSP00000508921.1:n.*225T>G
ENST00000686877.1:c.*763T>G (KRAS) ENSP00000510431.1:n.*763T>G
ENST00000687356.1:c.*490T>G (KRAS) ENSP00000510511.1:n.*490T>G
ENST00000688940.1:c.*225T>G (KRAS) ENSP00000509238.1:n.*225T>G
ENST00000690406.1:c.595T>G (KRAS)
ENST00000690804.1:c.*753T>G (KRAS) ENSP00000508568.1:n.*753T>G
ENST00000692768.1:c.*225T>G (KRAS) ENSP00000510254.1:n.*225T>G
ENST00000693229.1:c.*225T>G (KRAS) ENSP00000509223.1:n.*225T>G
ENST00000256078.10:c.*346T>G (KRAS) MANE Plus Clinical ENSP00000256078.5:n.*346T>G
ENST00000311936.8:c.*225T>G (KRAS) MANE Select ENSP00000308495.3:n.*225T>G
ENST00000553788.6:c.*307A>C (ETFRF1) ENSP00000451938.2:n.*307A>C
ENST00000256078.8:c.*346T>G (KRAS) ENSP00000256078.4:n.*346T>G
ENST00000311936.7:c.*225T>G (KRAS) ENSP00000308495.3:n.*225T>G
ENST00000553788.5:c.*307A>C (ETFRF1) ENSP00000451938.1:n.*307A>C
ENST00000557334.5:c.*225T>G (KRAS) ENSP00000452512.1:n.*225T>G
NM_004985.4:c.*225T>G (KRAS) NP_004976.2:n.*225T>G
NM_033360.3:c.*346T>G (KRAS) NP_203524.1:n.*346T>G
XM_011520653.1:c.*225T>G (KRAS) XP_011518955.1:n.*225T>G
XM_011520653.3:c.*225T>G (KRAS) XP_011518955.1:n.*225T>G
NM_001369786.1:c.*346T>G (KRAS) NP_001356715.1:n.*346T>G
NM_001369787.1:c.*225T>G (KRAS) NP_001356716.1:n.*225T>G
NM_004985.5:c.*225T>G (KRAS) MANE Select NP_004976.2:n.*225T>G
NM_033360.4:c.*346T>G (KRAS) MANE Plus Clinical NP_203524.1:n.*346T>G