Canonical Allele Identifier: CA16609691

Gene: KRAS

Linked Data

• ClinVar Variation Id: 40461
• ClinVar RCV Id: RCV000473918 ; RCV000994878
• dbSNP Id: rs121913527
• COSMIC: COSM5967494
• MyVariant Identifiers: chr12:g.25378562C>A (hg19) ; chr12:g.25225628C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225628C>A , CM000674.2:g.25225628C>A	GRCh38
NC_000012.11:g.25378562C>A , CM000674.1:g.25378562C>A	GRCh37
NC_000012.10:g.25269829C>A	NCBI36
NG_007524.1:g.30293G>T
NG_007524.2:g.30376G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-15717G>T	ENSP00000452512.1:n.112-15717G>T
ENST00000685328.1:c.436G>T	ENSP00000508921.1:p.Ala146Ser
ENST00000686877.1:c.*407G>T	ENSP00000510431.1:n.*407G>T
ENST00000687356.1:c.*134G>T	ENSP00000510511.1:n.*134G>T
ENST00000688228.1:n.910G>T
ENST00000688940.1:c.436G>T	ENSP00000509238.1:p.Ala146Ser
ENST00000690406.1:c.146G>T
ENST00000690804.1:c.*397G>T	ENSP00000508568.1:n.*397G>T
ENST00000692768.1:c.238G>T	ENSP00000510254.1:p.Ala80Ser
ENST00000693229.1:c.361G>T	ENSP00000509223.1:p.Ala121Ser
ENST00000256078.10:c.436G>T MANE Plus Clinical	ENSP00000256078.5:p.Ala146Ser
ENST00000311936.8:c.436G>T MANE Select	ENSP00000308495.3:p.Ala146Ser
ENST00000256078.8:c.436G>T	ENSP00000256078.4:p.Ala146Ser
ENST00000311936.7:c.436G>T	ENSP00000308495.3:p.Ala146Ser
ENST00000557334.5:c.112-15717G>T	ENSP00000452512.1:n.112-15717G>T
NM_004985.4:c.436G>T	NP_004976.2:p.Ala146Ser
NM_033360.3:c.436G>T	NP_203524.1:p.Ala146Ser
XM_006719069.2:c.436G>T	XP_006719132.1:p.Ala146Ser
XM_011520653.1:c.436G>T	XP_011518955.1:p.Ala146Ser
XM_006719069.4:c.436G>T	XP_006719132.1:p.Ala146Ser
XM_011520653.3:c.436G>T	XP_011518955.1:p.Ala146Ser
NM_001369786.1:c.436G>T	NP_001356715.1:p.Ala146Ser
NM_001369787.1:c.436G>T	NP_001356716.1:p.Ala146Ser
NM_004985.5:c.436G>T MANE Select	NP_004976.2:p.Ala146Ser
NM_033360.4:c.436G>T MANE Plus Clinical	NP_203524.1:p.Ala146Ser