Canonical Allele Identifier: CA2499221590

Gene: KRAS

Linked Data

• ClinVar Variation Id: 1264725
• ClinVar RCV Id: RCV001676970 ; RCV002073171
• dbSNP Id: rs2141481751

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209909A>G , CM000674.2:g.25209909A>G	GRCh38
NC_000012.11:g.25362843A>G , CM000674.1:g.25362843A>G	GRCh37
NC_000012.10:g.25254110A>G	NCBI36
NG_007524.1:g.46012T>C
NG_007524.2:g.46095T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.114T>C	ENSP00000452512.1:p.Gly38=
ENST00000685328.1:c.453T>C	ENSP00000508921.1:p.Gly151=
ENST00000686877.1:c.*424T>C	ENSP00000510431.1:n.*424T>C
ENST00000687356.1:c.*151T>C	ENSP00000510511.1:n.*151T>C
ENST00000688228.1:n.927T>C
ENST00000688940.1:c.453T>C	ENSP00000509238.1:p.Gly151=
ENST00000690406.1:c.256T>C
ENST00000690804.1:c.*414T>C	ENSP00000508568.1:n.*414T>C
ENST00000692768.1:c.255T>C	ENSP00000510254.1:p.Gly85=
ENST00000693229.1:c.378T>C	ENSP00000509223.1:p.Gly126=
ENST00000256078.10:c.*7T>C MANE Plus Clinical	ENSP00000256078.5:n.*7T>C
ENST00000311936.8:c.453T>C MANE Select	ENSP00000308495.3:p.Gly151=
ENST00000256078.8:c.*7T>C	ENSP00000256078.4:n.*7T>C
ENST00000311936.7:c.453T>C	ENSP00000308495.3:p.Gly151=
ENST00000557334.5:c.114T>C	ENSP00000452512.1:p.Gly38=
NM_004985.4:c.453T>C	NP_004976.2:p.Gly151=
NM_033360.3:c.*7T>C	NP_203524.1:n.*7T>C
XM_006719069.2:c.*7T>C	XP_006719132.1:n.*7T>C
XM_011520653.1:c.453T>C	XP_011518955.1:p.Gly151=
XM_006719069.4:c.*7T>C	XP_006719132.1:n.*7T>C
XM_011520653.3:c.453T>C	XP_011518955.1:p.Gly151=
NM_001369786.1:c.*7T>C	NP_001356715.1:n.*7T>C
NM_001369787.1:c.453T>C	NP_001356716.1:p.Gly151=
NM_004985.5:c.453T>C MANE Select	NP_004976.2:p.Gly151=
NM_033360.4:c.*7T>C MANE Plus Clinical	NP_203524.1:n.*7T>C