Canonical Allele Identifier: CA2617994084

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209603G>C , CM000674.2:g.25209603G>C GRCh38
NC_000012.11:g.25362537G>C , CM000674.1:g.25362537G>C GRCh37
NC_000012.10:g.25253804G>C NCBI36
NG_007524.1:g.46318C>G
NG_007524.2:g.46401C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000557334.6:c.*192C>G (KRAS) ENSP00000452512.1:n.*192C>G
ENST00000685328.1:c.*192C>G (KRAS) ENSP00000508921.1:n.*192C>G
ENST00000686877.1:c.*730C>G (KRAS) ENSP00000510431.1:n.*730C>G
ENST00000687356.1:c.*457C>G (KRAS) ENSP00000510511.1:n.*457C>G
ENST00000688940.1:c.*192C>G (KRAS) ENSP00000509238.1:n.*192C>G
ENST00000690406.1:c.562C>G (KRAS)
ENST00000690804.1:c.*720C>G (KRAS) ENSP00000508568.1:n.*720C>G
ENST00000692768.1:c.*192C>G (KRAS) ENSP00000510254.1:n.*192C>G
ENST00000693229.1:c.*192C>G (KRAS) ENSP00000509223.1:n.*192C>G
ENST00000256078.10:c.*313C>G (KRAS) MANE Plus Clinical ENSP00000256078.5:n.*313C>G
ENST00000311936.8:c.*192C>G (KRAS) MANE Select ENSP00000308495.3:n.*192C>G
ENST00000553788.6:c.*340G>C (ETFRF1) ENSP00000451938.2:n.*340G>C
ENST00000256078.8:c.*313C>G (KRAS) ENSP00000256078.4:n.*313C>G
ENST00000311936.7:c.*192C>G (KRAS) ENSP00000308495.3:n.*192C>G
ENST00000553788.5:c.*340G>C (ETFRF1) ENSP00000451938.1:n.*340G>C
ENST00000557334.5:c.*192C>G (KRAS) ENSP00000452512.1:n.*192C>G
NM_004985.4:c.*192C>G (KRAS) NP_004976.2:n.*192C>G
NM_033360.3:c.*313C>G (KRAS) NP_203524.1:n.*313C>G
XM_011520653.1:c.*192C>G (KRAS) XP_011518955.1:n.*192C>G
XM_011520653.3:c.*192C>G (KRAS) XP_011518955.1:n.*192C>G
NM_001369786.1:c.*313C>G (KRAS) NP_001356715.1:n.*313C>G
NM_001369787.1:c.*192C>G (KRAS) NP_001356716.1:n.*192C>G
NM_004985.5:c.*192C>G (KRAS) MANE Select NP_004976.2:n.*192C>G
NM_033360.4:c.*313C>G (KRAS) MANE Plus Clinical NP_203524.1:n.*313C>G