Canonical Allele Identifier: CA2794888727

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209903A>G , CM000674.2:g.25209903A>G	GRCh38
NC_000012.11:g.25362837A>G , CM000674.1:g.25362837A>G	GRCh37
NC_000012.10:g.25254104A>G	NCBI36
NG_007524.1:g.46018T>C
NG_007524.2:g.46101T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.120T>C	ENSP00000452512.1:p.Asp40=
ENST00000685328.1:c.459T>C	ENSP00000508921.1:p.Asp153=
ENST00000686877.1:c.*430T>C	ENSP00000510431.1:n.*430T>C
ENST00000687356.1:c.*157T>C	ENSP00000510511.1:n.*157T>C
ENST00000688228.1:n.933T>C
ENST00000688940.1:c.459T>C	ENSP00000509238.1:p.Asp153=
ENST00000690406.1:c.262T>C
ENST00000690804.1:c.*420T>C	ENSP00000508568.1:n.*420T>C
ENST00000692768.1:c.261T>C	ENSP00000510254.1:p.Asp87=
ENST00000693229.1:c.384T>C	ENSP00000509223.1:p.Asp128=
ENST00000256078.10:c.*13T>C MANE Plus Clinical	ENSP00000256078.5:n.*13T>C
ENST00000311936.8:c.459T>C MANE Select	ENSP00000308495.3:p.Asp153=
ENST00000256078.8:c.*13T>C	ENSP00000256078.4:n.*13T>C
ENST00000311936.7:c.459T>C	ENSP00000308495.3:p.Asp153=
ENST00000557334.5:c.120T>C	ENSP00000452512.1:p.Asp40=
NM_004985.4:c.459T>C	NP_004976.2:p.Asp153=
NM_033360.3:c.*13T>C	NP_203524.1:n.*13T>C
XM_006719069.2:c.*13T>C	XP_006719132.1:n.*13T>C
XM_011520653.1:c.459T>C	XP_011518955.1:p.Asp153=
XM_006719069.4:c.*13T>C	XP_006719132.1:n.*13T>C
XM_011520653.3:c.459T>C	XP_011518955.1:p.Asp153=
NM_001369786.1:c.*13T>C	NP_001356715.1:n.*13T>C
NM_001369787.1:c.459T>C	NP_001356716.1:p.Asp153=
NM_004985.5:c.459T>C MANE Select	NP_004976.2:p.Asp153=
NM_033360.4:c.*13T>C MANE Plus Clinical	NP_203524.1:n.*13T>C