Canonical Allele Identifier: CA6486821

Gene: KRAS

Linked Data

• ClinVar Variation Id: 1113732
• ClinVar RCV Id: RCV001441177
• dbSNP Id: rs749587181
• ExAC: 12:25362755 ACTT / A
• gnomAD v2: 12-25362755-ACTT-A
• gnomAD v3: 12-25209821-ACTT-A
• gnomAD v4: 12-25209821-ACTT-A
• COSMIC: COSM2202548
• MyVariant Identifiers: chr12:g.25362756_25362758del (hg19) ; chr12:g.25209822_25209824del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209825_25209827del , CM000674.2:g.25209825_25209827del	GRCh38
NC_000012.11:g.25362759_25362761del , CM000674.1:g.25362759_25362761del	GRCh37
NC_000012.10:g.25254026_25254028del	NCBI36
NG_007524.1:g.46097_46099del
NG_007524.2:g.46180_46182del

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.199_201del	ENSP00000452512.1:p.Lys67del
ENST00000685328.1:c.538_540del	ENSP00000508921.1:p.Lys180del
ENST00000686877.1:c.*509_*511del	ENSP00000510431.1:n.*509_*511del
ENST00000687356.1:c.*236_*238del	ENSP00000510511.1:n.*236_*238del
ENST00000688228.1:n.1012_1014del
ENST00000688940.1:c.538_540del	ENSP00000509238.1:p.Lys180del
ENST00000690406.1:c.341_343del
ENST00000690804.1:c.*499_*501del	ENSP00000508568.1:n.*499_*501del
ENST00000692768.1:c.340_342del	ENSP00000510254.1:p.Lys114del
ENST00000693229.1:c.463_465del	ENSP00000509223.1:p.Lys155del
ENST00000256078.10:c.*92_*94del MANE Plus Clinical	ENSP00000256078.5:n.*92_*94del
ENST00000311936.8:c.538_540del MANE Select	ENSP00000308495.3:p.Lys180del
ENST00000256078.8:c.*92_*94del	ENSP00000256078.4:n.*92_*94del
ENST00000311936.7:c.538_540del	ENSP00000308495.3:p.Lys180del
ENST00000557334.5:c.199_201del	ENSP00000452512.1:p.Lys67del
NM_004985.4:c.538_540del	NP_004976.2:p.Lys180del
NM_033360.3:c.*92_*94del	NP_203524.1:n.*92_*94del
XM_011520653.1:c.538_540del	XP_011518955.1:p.Lys180del
XM_011520653.3:c.538_540del	XP_011518955.1:p.Lys180del
NM_001369786.1:c.*92_*94del	NP_001356715.1:n.*92_*94del
NM_001369787.1:c.538_540del	NP_001356716.1:p.Lys180del
NM_004985.5:c.538_540del MANE Select	NP_004976.2:p.Lys180del
NM_033360.4:c.*92_*94del MANE Plus Clinical	NP_203524.1:n.*92_*94del