Canonical Allele Identifier: CA384148418

Gene: KRAS

Linked Data

• COSMIC: COSM5878677
• MyVariant Identifiers: chr12:g.25362789C>A (hg19) ; chr12:g.25209855C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209855C>A , CM000674.2:g.25209855C>A	GRCh38
NC_000012.11:g.25362789C>A , CM000674.1:g.25362789C>A	GRCh37
NC_000012.10:g.25254056C>A	NCBI36
NG_007524.1:g.46066G>T
NG_007524.2:g.46149G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.168G>T	ENSP00000452512.1:p.Lys56Asn
ENST00000685328.1:c.507G>T	ENSP00000508921.1:p.Lys169Asn
ENST00000686877.1:c.*478G>T	ENSP00000510431.1:n.*478G>T
ENST00000687356.1:c.*205G>T	ENSP00000510511.1:n.*205G>T
ENST00000688228.1:n.981G>T
ENST00000688940.1:c.507G>T	ENSP00000509238.1:p.Lys169Asn
ENST00000690406.1:c.310G>T
ENST00000690804.1:c.*468G>T	ENSP00000508568.1:n.*468G>T
ENST00000692768.1:c.309G>T	ENSP00000510254.1:p.Lys103Asn
ENST00000693229.1:c.432G>T	ENSP00000509223.1:p.Lys144Asn
ENST00000256078.10:c.*61G>T MANE Plus Clinical	ENSP00000256078.5:n.*61G>T
ENST00000311936.8:c.507G>T MANE Select	ENSP00000308495.3:p.Lys169Asn
ENST00000256078.8:c.*61G>T	ENSP00000256078.4:n.*61G>T
ENST00000311936.7:c.507G>T	ENSP00000308495.3:p.Lys169Asn
ENST00000557334.5:c.168G>T	ENSP00000452512.1:p.Lys56Asn
NM_004985.4:c.507G>T	NP_004976.2:p.Lys169Asn
NM_033360.3:c.*61G>T	NP_203524.1:n.*61G>T
XM_006719069.2:c.*61G>T	XP_006719132.1:n.*61G>T
XM_011520653.1:c.507G>T	XP_011518955.1:p.Lys169Asn
XM_006719069.4:c.*61G>T	XP_006719132.1:n.*61G>T
XM_011520653.3:c.507G>T	XP_011518955.1:p.Lys169Asn
NM_001369786.1:c.*61G>T	NP_001356715.1:n.*61G>T
NM_001369787.1:c.507G>T	NP_001356716.1:p.Lys169Asn
NM_004985.5:c.507G>T MANE Select	NP_004976.2:p.Lys169Asn
NM_033360.4:c.*61G>T MANE Plus Clinical	NP_203524.1:n.*61G>T