Canonical Allele Identifier: CA256484

Gene: KRAS

Linked Data

• ClinVar Variation Id: 12597
• ClinVar RCV Id: RCV000013428 ; RCV000157934 ; RCV000689097 ; RCV002470709
• dbSNP Id: rs104894359
• MyVariant Identifiers: chr12:g.25380280C>T (hg19) ; chr12:g.25227346C>T (hg38)
• PubMed: PMID:19396835

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25227346C>T , CM000674.2:g.25227346C>T	GRCh38
NC_000012.11:g.25380280C>T , CM000674.1:g.25380280C>T	GRCh37
NC_000012.10:g.25271547C>T	NCBI36
NG_007524.1:g.28575G>A
NG_007524.2:g.28658G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-17435G>A	ENSP00000452512.1:n.112-17435G>A
ENST00000685328.1:c.178G>A	ENSP00000508921.1:p.Gly60Ser
ENST00000686877.1:c.*149G>A	ENSP00000510431.1:n.*149G>A
ENST00000687356.1:c.112-1573G>A	ENSP00000510511.1:n.112-1573G>A
ENST00000688228.1:n.652G>A
ENST00000688940.1:c.178G>A	ENSP00000509238.1:p.Gly60Ser
ENST00000690804.1:c.*139G>A	ENSP00000508568.1:n.*139G>A
ENST00000692768.1:c.-21G>A	ENSP00000510254.1:n.-21G>A
ENST00000693229.1:c.112-9G>A	ENSP00000509223.1:n.112-9G>A
ENST00000256078.10:c.178G>A MANE Plus Clinical	ENSP00000256078.5:p.Gly60Ser
ENST00000311936.8:c.178G>A MANE Select	ENSP00000308495.3:p.Gly60Ser
ENST00000256078.8:c.178G>A	ENSP00000256078.4:p.Gly60Ser
ENST00000311936.7:c.178G>A	ENSP00000308495.3:p.Gly60Ser
ENST00000557334.5:c.112-17435G>A	ENSP00000452512.1:n.112-17435G>A
NM_004985.4:c.178G>A	NP_004976.2:p.Gly60Ser
NM_033360.3:c.178G>A	NP_203524.1:p.Gly60Ser
XM_006719069.2:c.178G>A	XP_006719132.1:p.Gly60Ser
XM_011520653.1:c.178G>A	XP_011518955.1:p.Gly60Ser
XM_006719069.4:c.178G>A	XP_006719132.1:p.Gly60Ser
XM_011520653.3:c.178G>A	XP_011518955.1:p.Gly60Ser
NM_001369786.1:c.178G>A	NP_001356715.1:p.Gly60Ser
NM_001369787.1:c.178G>A	NP_001356716.1:p.Gly60Ser
NM_004985.5:c.178G>A MANE Select	NP_004976.2:p.Gly60Ser
NM_033360.4:c.178G>A MANE Plus Clinical	NP_203524.1:p.Gly60Ser