Canonical Allele Identifier: CA384148282

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25362733A>C (hg19) ; chr12:g.25209799A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.224T>G	ENSP00000452512.1:p.Met75Arg
ENST00000685328.1:c.563T>G	ENSP00000508921.1:p.Met188Arg
ENST00000686877.1:c.*534T>G	ENSP00000510431.1:n.*534T>G
ENST00000687356.1:c.*261T>G	ENSP00000510511.1:n.*261T>G
ENST00000688228.1:n.1037T>G
ENST00000688940.1:c.563T>G	ENSP00000509238.1:p.Met188Arg
ENST00000690406.1:c.366T>G
ENST00000690804.1:c.*524T>G	ENSP00000508568.1:n.*524T>G
ENST00000692768.1:c.365T>G	ENSP00000510254.1:p.Met122Arg
ENST00000693229.1:c.488T>G	ENSP00000509223.1:p.Met163Arg
ENST00000256078.10:c.*117T>G MANE Plus Clinical	ENSP00000256078.5:n.*117T>G
ENST00000311936.8:c.563T>G MANE Select	ENSP00000308495.3:p.Met188Arg
ENST00000256078.8:c.*117T>G	ENSP00000256078.4:n.*117T>G
ENST00000311936.7:c.563T>G	ENSP00000308495.3:p.Met188Arg
ENST00000557334.5:c.224T>G	ENSP00000452512.1:p.Met75Arg
NM_004985.4:c.563T>G	NP_004976.2:p.Met188Arg
NM_033360.3:c.*117T>G	NP_203524.1:n.*117T>G
XM_011520653.1:c.563T>G	XP_011518955.1:p.Met188Arg
XM_011520653.3:c.563T>G	XP_011518955.1:p.Met188Arg
NM_001369786.1:c.*117T>G	NP_001356715.1:n.*117T>G
NM_001369787.1:c.563T>G	NP_001356716.1:p.Met188Arg
NM_004985.5:c.563T>G MANE Select	NP_004976.2:p.Met188Arg
NM_033360.4:c.*117T>G MANE Plus Clinical	NP_203524.1:n.*117T>G