Canonical Allele Identifier: CA384149222
Gene: KRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25215543A>C , CM000674.2:g.25215543A>C GRCh38
NC_000012.11:g.25368477A>C , CM000674.1:g.25368477A>C GRCh37
NC_000012.10:g.25259744A>C NCBI36
NG_007524.1:g.40378T>G
NG_007524.2:g.40461T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000256078.10:c.468T>G ENSP00000256078.5:p.Phe156Leu
ENST00000311936.8:c.451-5632T>G MANE Select ENSP00000308495.3:p.=
ENST00000256078.8:c.468T>G ENSP00000256078.4:p.Phe156Leu
ENST00000311936.7:c.451-5632T>G ENSP00000308495.3:p.=
ENST00000557334.5:c.112-5632T>G ENSP00000452512.1:p.=
NM_004985.4:c.451-5632T>G NP_004976.2:p.=
NM_033360.3:c.468T>G NP_203524.1:p.Phe156Leu
XM_006719069.2:c.468T>G XP_006719132.1:p.Phe156Leu
XM_011520653.1:c.451-5632T>G XP_011518955.1:p.=
XM_006719069.4:c.468T>G XP_006719132.1:p.Phe156Leu
XM_011520653.3:c.451-5632T>G XP_011518955.1:p.=
NM_001369786.1:c.468T>G NP_001356715.1:p.Phe156Leu
NM_001369787.1:c.451-5632T>G NP_001356716.1:p.=
NM_004985.5:c.451-5632T>G MANE Select NP_004976.2:p.=
NM_033360.4:c.468T>G NP_203524.1:p.Phe156Leu