Canonical Allele Identifier: CA234206747

Linked Data

dbSNP Id: rs917782865

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209631dup , CM000674.2:g.25209631dup GRCh38
NC_000012.11:g.25362565dup , CM000674.1:g.25362565dup GRCh37
NC_000012.10:g.25253832dup NCBI36
NG_007524.1:g.46298dup
NG_007524.2:g.46381dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000557334.6:c.*172dup (KRAS) ENSP00000452512.1:n.*172dup
ENST00000685328.1:c.*172dup (KRAS) ENSP00000508921.1:n.*172dup
ENST00000686877.1:c.*710dup (KRAS) ENSP00000510431.1:n.*710dup
ENST00000687356.1:c.*437dup (KRAS) ENSP00000510511.1:n.*437dup
ENST00000688940.1:c.*172dup (KRAS) ENSP00000509238.1:n.*172dup
ENST00000690406.1:c.542dup (KRAS)
ENST00000690804.1:c.*700dup (KRAS) ENSP00000508568.1:n.*700dup
ENST00000692768.1:c.*172dup (KRAS) ENSP00000510254.1:n.*172dup
ENST00000693229.1:c.*172dup (KRAS) ENSP00000509223.1:n.*172dup
ENST00000256078.10:c.*293dup (KRAS) MANE Plus Clinical ENSP00000256078.5:n.*293dup
ENST00000311936.8:c.*172dup (KRAS) MANE Select ENSP00000308495.3:n.*172dup
ENST00000553788.6:c.*368dup (ETFRF1) ENSP00000451938.2:n.*368dup
ENST00000256078.8:c.*293dup (KRAS) ENSP00000256078.4:n.*293dup
ENST00000311936.7:c.*172dup (KRAS) ENSP00000308495.3:n.*172dup
ENST00000553788.5:c.*368dup (ETFRF1) ENSP00000451938.1:n.*368dup
ENST00000557334.5:c.*172dup (KRAS) ENSP00000452512.1:n.*172dup
NM_004985.4:c.*172dup (KRAS) NP_004976.2:n.*172dup
NM_033360.3:c.*293dup (KRAS) NP_203524.1:n.*293dup
XM_011520653.1:c.*172dup (KRAS) XP_011518955.1:n.*172dup
XM_011520653.3:c.*172dup (KRAS) XP_011518955.1:n.*172dup
NM_001369786.1:c.*293dup (KRAS) NP_001356715.1:n.*293dup
NM_001369787.1:c.*172dup (KRAS) NP_001356716.1:n.*172dup
NM_004985.5:c.*172dup (KRAS) MANE Select NP_004976.2:n.*172dup
NM_033360.4:c.*293dup (KRAS) MANE Plus Clinical NP_203524.1:n.*293dup