Canonical Allele Identifier: CA478890263

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25380218A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25227284A>G , CM000674.2:g.25227284A>G	GRCh38
NC_000012.11:g.25380218A>G , CM000674.1:g.25380218A>G	GRCh37
NC_000012.10:g.25271485A>G	NCBI36
NG_007524.1:g.28637T>C
NG_007524.2:g.28720T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-17373T>C	ENSP00000452512.1:n.112-17373T>C
ENST00000685328.1:c.240T>C	ENSP00000508921.1:p.Cys80=
ENST00000686877.1:c.*211T>C	ENSP00000510431.1:n.*211T>C
ENST00000687356.1:c.112-1511T>C	ENSP00000510511.1:n.112-1511T>C
ENST00000688228.1:n.714T>C
ENST00000688940.1:c.240T>C	ENSP00000509238.1:p.Cys80=
ENST00000690804.1:c.*201T>C	ENSP00000508568.1:n.*201T>C
ENST00000692768.1:c.42T>C	ENSP00000510254.1:p.Cys14=
ENST00000693229.1:c.165T>C	ENSP00000509223.1:p.Cys55=
ENST00000256078.10:c.240T>C MANE Plus Clinical	ENSP00000256078.5:p.Cys80=
ENST00000311936.8:c.240T>C MANE Select	ENSP00000308495.3:p.Cys80=
ENST00000256078.8:c.240T>C	ENSP00000256078.4:p.Cys80=
ENST00000311936.7:c.240T>C	ENSP00000308495.3:p.Cys80=
ENST00000557334.5:c.112-17373T>C	ENSP00000452512.1:n.112-17373T>C
NM_004985.4:c.240T>C	NP_004976.2:p.Cys80=
NM_033360.3:c.240T>C	NP_203524.1:p.Cys80=
XM_006719069.2:c.240T>C	XP_006719132.1:p.Cys80=
XM_011520653.1:c.240T>C	XP_011518955.1:p.Cys80=
XM_006719069.4:c.240T>C	XP_006719132.1:p.Cys80=
XM_011520653.3:c.240T>C	XP_011518955.1:p.Cys80=
NM_001369786.1:c.240T>C	NP_001356715.1:p.Cys80=
NM_001369787.1:c.240T>C	NP_001356716.1:p.Cys80=
NM_004985.5:c.240T>C MANE Select	NP_004976.2:p.Cys80=
NM_033360.4:c.240T>C MANE Plus Clinical	NP_203524.1:p.Cys80=