Canonical Allele Identifier: CA478890128

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25378694T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225760T>G , CM000674.2:g.25225760T>G	GRCh38
NC_000012.11:g.25378694T>G , CM000674.1:g.25378694T>G	GRCh37
NC_000012.10:g.25269961T>G	NCBI36
NG_007524.1:g.30161A>C
NG_007524.2:g.30244A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15849A>C	ENSP00000452512.1:n.112-15849A>C
ENST00000685328.1:c.304A>C	ENSP00000508921.1:p.Arg102=
ENST00000686877.1:c.*275A>C	ENSP00000510431.1:n.*275A>C
ENST00000687356.1:c.*2A>C	ENSP00000510511.1:n.*2A>C
ENST00000688228.1:n.778A>C
ENST00000688940.1:c.304A>C	ENSP00000509238.1:p.Arg102=
ENST00000690406.1:c.14A>C
ENST00000690804.1:c.*265A>C	ENSP00000508568.1:n.*265A>C
ENST00000692768.1:c.106A>C	ENSP00000510254.1:p.Arg36=
ENST00000693229.1:c.229A>C	ENSP00000509223.1:p.Arg77=
ENST00000256078.10:c.304A>C MANE Plus Clinical	ENSP00000256078.5:p.Arg102=
ENST00000311936.8:c.304A>C MANE Select	ENSP00000308495.3:p.Arg102=
ENST00000256078.8:c.304A>C	ENSP00000256078.4:p.Arg102=
ENST00000311936.7:c.304A>C	ENSP00000308495.3:p.Arg102=
ENST00000557334.5:c.112-15849A>C	ENSP00000452512.1:n.112-15849A>C
NM_004985.4:c.304A>C	NP_004976.2:p.Arg102=
NM_033360.3:c.304A>C	NP_203524.1:p.Arg102=
XM_006719069.2:c.304A>C	XP_006719132.1:p.Arg102=
XM_011520653.1:c.304A>C	XP_011518955.1:p.Arg102=
XM_006719069.4:c.304A>C	XP_006719132.1:p.Arg102=
XM_011520653.3:c.304A>C	XP_011518955.1:p.Arg102=
NM_001369786.1:c.304A>C	NP_001356715.1:p.Arg102=
NM_001369787.1:c.304A>C	NP_001356716.1:p.Arg102=
NM_004985.5:c.304A>C MANE Select	NP_004976.2:p.Arg102=
NM_033360.4:c.304A>C MANE Plus Clinical	NP_203524.1:p.Arg102=