Canonical Allele Identifier: CA2617998742

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25206275C>A , CM000674.2:g.25206275C>A GRCh38
NC_000012.11:g.25359209C>A , CM000674.1:g.25359209C>A GRCh37
NC_000012.10:g.25250476C>A NCBI36
NG_007524.1:g.49646G>T
NG_007524.2:g.49729G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000685328.1:c.*3520G>T (KRAS) ENSP00000508921.1:n.*3520G>T
ENST00000686877.1:c.*4058G>T (KRAS) ENSP00000510431.1:n.*4058G>T
ENST00000687356.1:c.*3785G>T (KRAS) ENSP00000510511.1:n.*3785G>T
ENST00000690406.1:c.3890G>T (KRAS)
ENST00000692768.1:c.*3520G>T (KRAS) ENSP00000510254.1:n.*3520G>T
ENST00000693229.1:c.*3520G>T (KRAS) ENSP00000509223.1:n.*3520G>T
ENST00000256078.10:c.*3641G>T (KRAS) MANE Plus Clinical ENSP00000256078.5:n.*3641G>T
ENST00000311936.8:c.*3520G>T (KRAS) MANE Select ENSP00000308495.3:n.*3520G>T
ENST00000553788.6:c.51+2268C>A (ETFRF1) ENSP00000451938.2:n.51+2268C>A
ENST00000311936.7:c.*3520G>T (KRAS) ENSP00000308495.3:n.*3520G>T
ENST00000553788.5:c.45+2268C>A (ETFRF1) ENSP00000451938.1:n.45+2268C>A
NM_004985.4:c.*3520G>T (KRAS) NP_004976.2:n.*3520G>T
NM_033360.3:c.*3641G>T (KRAS) NP_203524.1:n.*3641G>T
XM_011520653.1:c.*3520G>T (KRAS) XP_011518955.1:n.*3520G>T
XM_011520653.3:c.*3520G>T (KRAS) XP_011518955.1:n.*3520G>T
NM_001369786.1:c.*3641G>T (KRAS) NP_001356715.1:n.*3641G>T
NM_001369787.1:c.*3520G>T (KRAS) NP_001356716.1:n.*3520G>T
NM_004985.5:c.*3520G>T (KRAS) MANE Select NP_004976.2:n.*3520G>T
NM_033360.4:c.*3641G>T (KRAS) MANE Plus Clinical NP_203524.1:n.*3641G>T