Canonical Allele Identifier: CA384148283

Gene: KRAS

Linked Data

• ClinVar Variation Id: 2086297
• ClinVar RCV Id: RCV003015448
• MyVariant Identifiers: chr12:g.25362733A>G (hg19) ; chr12:g.25209799A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209799A>G , CM000674.2:g.25209799A>G	GRCh38
NC_000012.11:g.25362733A>G , CM000674.1:g.25362733A>G	GRCh37
NC_000012.10:g.25254000A>G	NCBI36
NG_007524.1:g.46122T>C
NG_007524.2:g.46205T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.224T>C	ENSP00000452512.1:p.Met75Thr
ENST00000685328.1:c.563T>C	ENSP00000508921.1:p.Met188Thr
ENST00000686877.1:c.*534T>C	ENSP00000510431.1:n.*534T>C
ENST00000687356.1:c.*261T>C	ENSP00000510511.1:n.*261T>C
ENST00000688228.1:n.1037T>C
ENST00000688940.1:c.563T>C	ENSP00000509238.1:p.Met188Thr
ENST00000690406.1:c.366T>C
ENST00000690804.1:c.*524T>C	ENSP00000508568.1:n.*524T>C
ENST00000692768.1:c.365T>C	ENSP00000510254.1:p.Met122Thr
ENST00000693229.1:c.488T>C	ENSP00000509223.1:p.Met163Thr
ENST00000256078.10:c.*117T>C MANE Plus Clinical	ENSP00000256078.5:n.*117T>C
ENST00000311936.8:c.563T>C MANE Select	ENSP00000308495.3:p.Met188Thr
ENST00000256078.8:c.*117T>C	ENSP00000256078.4:n.*117T>C
ENST00000311936.7:c.563T>C	ENSP00000308495.3:p.Met188Thr
ENST00000557334.5:c.224T>C	ENSP00000452512.1:p.Met75Thr
NM_004985.4:c.563T>C	NP_004976.2:p.Met188Thr
NM_033360.3:c.*117T>C	NP_203524.1:n.*117T>C
XM_011520653.1:c.563T>C	XP_011518955.1:p.Met188Thr
XM_011520653.3:c.563T>C	XP_011518955.1:p.Met188Thr
NM_001369786.1:c.*117T>C	NP_001356715.1:n.*117T>C
NM_001369787.1:c.563T>C	NP_001356716.1:p.Met188Thr
NM_004985.5:c.563T>C MANE Select	NP_004976.2:p.Met188Thr
NM_033360.4:c.*117T>C MANE Plus Clinical	NP_203524.1:n.*117T>C