Canonical Allele Identifier: CA478890025

Gene: KRAS

Linked Data

• dbSNP Id: rs1951383711
• MyVariant Identifiers: chr12:g.25378608A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225674A>G , CM000674.2:g.25225674A>G	GRCh38
NC_000012.11:g.25378608A>G , CM000674.1:g.25378608A>G	GRCh37
NC_000012.10:g.25269875A>G	NCBI36
NG_007524.1:g.30247T>C
NG_007524.2:g.30330T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15763T>C	ENSP00000452512.1:n.112-15763T>C
ENST00000685328.1:c.390T>C	ENSP00000508921.1:p.Ala130=
ENST00000686877.1:c.*361T>C	ENSP00000510431.1:n.*361T>C
ENST00000687356.1:c.*88T>C	ENSP00000510511.1:n.*88T>C
ENST00000688228.1:n.864T>C
ENST00000688940.1:c.390T>C	ENSP00000509238.1:p.Ala130=
ENST00000690406.1:c.100T>C
ENST00000690804.1:c.*351T>C	ENSP00000508568.1:n.*351T>C
ENST00000692768.1:c.192T>C	ENSP00000510254.1:p.Ala64=
ENST00000693229.1:c.315T>C	ENSP00000509223.1:p.Ala105=
ENST00000256078.10:c.390T>C MANE Plus Clinical	ENSP00000256078.5:p.Ala130=
ENST00000311936.8:c.390T>C MANE Select	ENSP00000308495.3:p.Ala130=
ENST00000256078.8:c.390T>C	ENSP00000256078.4:p.Ala130=
ENST00000311936.7:c.390T>C	ENSP00000308495.3:p.Ala130=
ENST00000557334.5:c.112-15763T>C	ENSP00000452512.1:n.112-15763T>C
NM_004985.4:c.390T>C	NP_004976.2:p.Ala130=
NM_033360.3:c.390T>C	NP_203524.1:p.Ala130=
XM_006719069.2:c.390T>C	XP_006719132.1:p.Ala130=
XM_011520653.1:c.390T>C	XP_011518955.1:p.Ala130=
XM_006719069.4:c.390T>C	XP_006719132.1:p.Ala130=
XM_011520653.3:c.390T>C	XP_011518955.1:p.Ala130=
NM_001369786.1:c.390T>C	NP_001356715.1:p.Ala130=
NM_001369787.1:c.390T>C	NP_001356716.1:p.Ala130=
NM_004985.5:c.390T>C MANE Select	NP_004976.2:p.Ala130=
NM_033360.4:c.390T>C MANE Plus Clinical	NP_203524.1:p.Ala130=