Canonical Allele Identifier: CA384148288

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25362735A>C (hg19) ; chr12:g.25209801A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209801A>C , CM000674.2:g.25209801A>C	GRCh38
NC_000012.11:g.25362735A>C , CM000674.1:g.25362735A>C	GRCh37
NC_000012.10:g.25254002A>C	NCBI36
NG_007524.1:g.46120T>G
NG_007524.2:g.46203T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.222T>G	ENSP00000452512.1:p.Ile74Met
ENST00000685328.1:c.561T>G	ENSP00000508921.1:p.Ile187Met
ENST00000686877.1:c.*532T>G	ENSP00000510431.1:n.*532T>G
ENST00000687356.1:c.*259T>G	ENSP00000510511.1:n.*259T>G
ENST00000688228.1:n.1035T>G
ENST00000688940.1:c.561T>G	ENSP00000509238.1:p.Ile187Met
ENST00000690406.1:c.364T>G
ENST00000690804.1:c.*522T>G	ENSP00000508568.1:n.*522T>G
ENST00000692768.1:c.363T>G	ENSP00000510254.1:p.Ile121Met
ENST00000693229.1:c.486T>G	ENSP00000509223.1:p.Ile162Met
ENST00000256078.10:c.*115T>G MANE Plus Clinical	ENSP00000256078.5:n.*115T>G
ENST00000311936.8:c.561T>G MANE Select	ENSP00000308495.3:p.Ile187Met
ENST00000256078.8:c.*115T>G	ENSP00000256078.4:n.*115T>G
ENST00000311936.7:c.561T>G	ENSP00000308495.3:p.Ile187Met
ENST00000557334.5:c.222T>G	ENSP00000452512.1:p.Ile74Met
NM_004985.4:c.561T>G	NP_004976.2:p.Ile187Met
NM_033360.3:c.*115T>G	NP_203524.1:n.*115T>G
XM_011520653.1:c.561T>G	XP_011518955.1:p.Ile187Met
XM_011520653.3:c.561T>G	XP_011518955.1:p.Ile187Met
NM_001369786.1:c.*115T>G	NP_001356715.1:n.*115T>G
NM_001369787.1:c.561T>G	NP_001356716.1:p.Ile187Met
NM_004985.5:c.561T>G MANE Select	NP_004976.2:p.Ile187Met
NM_033360.4:c.*115T>G MANE Plus Clinical	NP_203524.1:n.*115T>G