Canonical Allele Identifier: CA384148289
Gene: KRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209802A>C , CM000674.2:g.25209802A>C GRCh38
NC_000012.11:g.25362736A>C , CM000674.1:g.25362736A>C GRCh37
NC_000012.10:g.25254003A>C NCBI36
NG_007524.1:g.46119T>G
NG_007524.2:g.46202T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.221T>G ENSP00000452512.1:p.Ile74Ser
ENST00000685328.1:c.560T>G ENSP00000508921.1:p.Ile187Ser
ENST00000686877.1:c.*531T>G ENSP00000510431.1:n.*531T>G
ENST00000687356.1:c.*258T>G ENSP00000510511.1:n.*258T>G
ENST00000688228.1:n.1034T>G
ENST00000688940.1:c.560T>G ENSP00000509238.1:p.Ile187Ser
ENST00000690406.1:c.363T>G
ENST00000690804.1:c.*521T>G ENSP00000508568.1:n.*521T>G
ENST00000692768.1:c.362T>G ENSP00000510254.1:p.Ile121Ser
ENST00000693229.1:c.485T>G ENSP00000509223.1:p.Ile162Ser
ENST00000256078.10:c.*114T>G MANE Plus Clinical ENSP00000256078.5:n.*114T>G
ENST00000311936.8:c.560T>G MANE Select ENSP00000308495.3:p.Ile187Ser
ENST00000256078.8:c.*114T>G ENSP00000256078.4:n.*114T>G
ENST00000311936.7:c.560T>G ENSP00000308495.3:p.Ile187Ser
ENST00000557334.5:c.221T>G ENSP00000452512.1:p.Ile74Ser
NM_004985.4:c.560T>G NP_004976.2:p.Ile187Ser
NM_033360.3:c.*114T>G NP_203524.1:n.*114T>G
XM_011520653.1:c.560T>G XP_011518955.1:p.Ile187Ser
XM_011520653.3:c.560T>G XP_011518955.1:p.Ile187Ser
NM_001369786.1:c.*114T>G NP_001356715.1:n.*114T>G
NM_001369787.1:c.560T>G NP_001356716.1:p.Ile187Ser
NM_004985.5:c.560T>G MANE Select NP_004976.2:p.Ile187Ser
NM_033360.4:c.*114T>G MANE Plus Clinical NP_203524.1:n.*114T>G