Canonical Allele Identifier: CA384151755

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25380189A>C (hg19) ; chr12:g.25227255A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25227255A>C , CM000674.2:g.25227255A>C	GRCh38
NC_000012.11:g.25380189A>C , CM000674.1:g.25380189A>C	GRCh37
NC_000012.10:g.25271456A>C	NCBI36
NG_007524.1:g.28666T>G
NG_007524.2:g.28749T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-17344T>G	ENSP00000452512.1:n.112-17344T>G
ENST00000685328.1:c.269T>G	ENSP00000508921.1:p.Phe90Cys
ENST00000686877.1:c.*240T>G	ENSP00000510431.1:n.*240T>G
ENST00000687356.1:c.112-1482T>G	ENSP00000510511.1:n.112-1482T>G
ENST00000688228.1:n.743T>G
ENST00000688940.1:c.269T>G	ENSP00000509238.1:p.Phe90Cys
ENST00000690804.1:c.*230T>G	ENSP00000508568.1:n.*230T>G
ENST00000692768.1:c.71T>G	ENSP00000510254.1:p.Phe24Cys
ENST00000693229.1:c.194T>G	ENSP00000509223.1:p.Phe65Cys
ENST00000256078.10:c.269T>G MANE Plus Clinical	ENSP00000256078.5:p.Phe90Cys
ENST00000311936.8:c.269T>G MANE Select	ENSP00000308495.3:p.Phe90Cys
ENST00000256078.8:c.269T>G	ENSP00000256078.4:p.Phe90Cys
ENST00000311936.7:c.269T>G	ENSP00000308495.3:p.Phe90Cys
ENST00000557334.5:c.112-17344T>G	ENSP00000452512.1:n.112-17344T>G
NM_004985.4:c.269T>G	NP_004976.2:p.Phe90Cys
NM_033360.3:c.269T>G	NP_203524.1:p.Phe90Cys
XM_006719069.2:c.269T>G	XP_006719132.1:p.Phe90Cys
XM_011520653.1:c.269T>G	XP_011518955.1:p.Phe90Cys
XM_006719069.4:c.269T>G	XP_006719132.1:p.Phe90Cys
XM_011520653.3:c.269T>G	XP_011518955.1:p.Phe90Cys
NM_001369786.1:c.269T>G	NP_001356715.1:p.Phe90Cys
NM_001369787.1:c.269T>G	NP_001356716.1:p.Phe90Cys
NM_004985.5:c.269T>G MANE Select	NP_004976.2:p.Phe90Cys
NM_033360.4:c.269T>G MANE Plus Clinical	NP_203524.1:p.Phe90Cys