Canonical Allele Identifier: CA384157449
Gene: KRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25245344A>C , CM000674.2:g.25245344A>C GRCh38
NC_000012.11:g.25398278A>C , CM000674.1:g.25398278A>C GRCh37
NC_000012.10:g.25289545A>C NCBI36
NG_007524.1:g.10577T>G
NG_007524.2:g.10660T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000556131.2:c.41T>G ENSP00000451856.1:p.Val14Gly
ENST00000557334.6:c.41T>G ENSP00000452512.1:p.Val14Gly
ENST00000685328.1:c.41T>G ENSP00000508921.1:p.Val14Gly
ENST00000686877.1:c.41T>G ENSP00000510431.1:p.Val14Gly
ENST00000686969.1:c.41T>G ENSP00000510479.1:p.Val14Gly
ENST00000687356.1:c.41T>G ENSP00000510511.1:p.Val14Gly
ENST00000688940.1:c.41T>G ENSP00000509238.1:p.Val14Gly
ENST00000690804.1:c.41T>G ENSP00000508568.1:p.Val14Gly
ENST00000692768.1:c.-88+5407T>G ENSP00000510254.1:n.-88+5407T>G
ENST00000693229.1:c.41T>G ENSP00000509223.1:p.Val14Gly
ENST00000256078.10:c.41T>G ENSP00000256078.5:p.Val14Gly
ENST00000311936.8:c.41T>G MANE Select ENSP00000308495.3:p.Val14Gly
ENST00000256078.8:c.41T>G ENSP00000256078.4:p.Val14Gly
ENST00000311936.7:c.41T>G ENSP00000308495.3:p.Val14Gly
ENST00000556131.1:c.41T>G ENSP00000451856.1:p.Val14Gly
ENST00000557334.5:c.41T>G ENSP00000452512.1:p.Val14Gly
NM_004985.4:c.41T>G NP_004976.2:p.Val14Gly
NM_033360.3:c.41T>G NP_203524.1:p.Val14Gly
XM_006719069.2:c.41T>G XP_006719132.1:p.Val14Gly
XM_011520653.1:c.41T>G XP_011518955.1:p.Val14Gly
XM_006719069.4:c.41T>G XP_006719132.1:p.Val14Gly
XM_011520653.3:c.41T>G XP_011518955.1:p.Val14Gly
NM_001369786.1:c.41T>G NP_001356715.1:p.Val14Gly
NM_001369787.1:c.41T>G NP_001356716.1:p.Val14Gly
NM_004985.5:c.41T>G MANE Select NP_004976.2:p.Val14Gly
NM_033360.4:c.41T>G NP_203524.1:p.Val14Gly