Canonical Allele Identifier: CA296084

Gene: KRAS

Linked Data

• ClinVar Variation Id: 40460
• ClinVar RCV Id: RCV000157937 ; RCV000999628 ; RCV000850568 ; RCV001269478
• dbSNP Id: rs730880471
• MyVariant Identifiers: chr12:g.25378643C>T (hg19) ; chr12:g.25225709C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225709C>T , CM000674.2:g.25225709C>T	GRCh38
NC_000012.11:g.25378643C>T , CM000674.1:g.25378643C>T	GRCh37
NC_000012.10:g.25269910C>T	NCBI36
NG_007524.1:g.30212G>A
NG_007524.2:g.30295G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15798G>A	ENSP00000452512.1:n.112-15798G>A
ENST00000685328.1:c.355G>A	ENSP00000508921.1:p.Asp119Asn
ENST00000686877.1:c.*326G>A	ENSP00000510431.1:n.*326G>A
ENST00000687356.1:c.*53G>A	ENSP00000510511.1:n.*53G>A
ENST00000688228.1:n.829G>A
ENST00000688940.1:c.355G>A	ENSP00000509238.1:p.Asp119Asn
ENST00000690406.1:c.65G>A
ENST00000690804.1:c.*316G>A	ENSP00000508568.1:n.*316G>A
ENST00000692768.1:c.157G>A	ENSP00000510254.1:p.Asp53Asn
ENST00000693229.1:c.280G>A	ENSP00000509223.1:p.Asp94Asn
ENST00000256078.10:c.355G>A MANE Plus Clinical	ENSP00000256078.5:p.Asp119Asn
ENST00000311936.8:c.355G>A MANE Select	ENSP00000308495.3:p.Asp119Asn
ENST00000256078.8:c.355G>A	ENSP00000256078.4:p.Asp119Asn
ENST00000311936.7:c.355G>A	ENSP00000308495.3:p.Asp119Asn
ENST00000557334.5:c.112-15798G>A	ENSP00000452512.1:n.112-15798G>A
NM_004985.4:c.355G>A	NP_004976.2:p.Asp119Asn
NM_033360.3:c.355G>A	NP_203524.1:p.Asp119Asn
XM_006719069.2:c.355G>A	XP_006719132.1:p.Asp119Asn
XM_011520653.1:c.355G>A	XP_011518955.1:p.Asp119Asn
XM_006719069.4:c.355G>A	XP_006719132.1:p.Asp119Asn
XM_011520653.3:c.355G>A	XP_011518955.1:p.Asp119Asn
NM_001369786.1:c.355G>A	NP_001356715.1:p.Asp119Asn
NM_001369787.1:c.355G>A	NP_001356716.1:p.Asp119Asn
NM_004985.5:c.355G>A MANE Select	NP_004976.2:p.Asp119Asn
NM_033360.4:c.355G>A MANE Plus Clinical	NP_203524.1:p.Asp119Asn