Canonical Allele Identifier: CA2617994540

Gene: KRAS

Linked Data

• dbSNP Id: rs1373386042
• gnomAD v4: 12-25209825-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209830del , CM000674.2:g.25209830del	GRCh38
NC_000012.11:g.25362764del , CM000674.1:g.25362764del	GRCh37
NC_000012.10:g.25254031del	NCBI36
NG_007524.1:g.46095del
NG_007524.2:g.46178del

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.197del	ENSP00000452512.1:p.Lys66ArgfsTer8
ENST00000685328.1:c.536del	ENSP00000508921.1:p.Lys179ArgfsTer8
ENST00000686877.1:c.*507del	ENSP00000510431.1:n.*507del
ENST00000687356.1:c.*234del	ENSP00000510511.1:n.*234del
ENST00000688228.1:n.1010del
ENST00000688940.1:c.536del	ENSP00000509238.1:p.Lys179ArgfsTer8
ENST00000690406.1:c.339del
ENST00000690804.1:c.*497del	ENSP00000508568.1:n.*497del
ENST00000692768.1:c.338del	ENSP00000510254.1:p.Lys113ArgfsTer8
ENST00000693229.1:c.461del	ENSP00000509223.1:p.Lys154ArgfsTer8
ENST00000256078.10:c.*90del MANE Plus Clinical	ENSP00000256078.5:n.*90del
ENST00000311936.8:c.536del MANE Select	ENSP00000308495.3:p.Lys179ArgfsTer8
ENST00000256078.8:c.*90del	ENSP00000256078.4:n.*90del
ENST00000311936.7:c.536del	ENSP00000308495.3:p.Lys179ArgfsTer8
ENST00000557334.5:c.197del	ENSP00000452512.1:p.Lys66ArgfsTer8
NM_004985.4:c.536del	NP_004976.2:p.Lys179ArgfsTer8
NM_033360.3:c.*90del	NP_203524.1:n.*90del
XM_006719069.2:c.*90del	XP_006719132.1:n.*90del
XM_011520653.1:c.536del	XP_011518955.1:p.Lys179ArgfsTer8
XM_006719069.4:c.*90del	XP_006719132.1:n.*90del
XM_011520653.3:c.536del	XP_011518955.1:p.Lys179ArgfsTer8
NM_001369786.1:c.*90del	NP_001356715.1:n.*90del
NM_001369787.1:c.536del	NP_001356716.1:p.Lys179ArgfsTer8
NM_004985.5:c.536del MANE Select	NP_004976.2:p.Lys179ArgfsTer8
NM_033360.4:c.*90del MANE Plus Clinical	NP_203524.1:n.*90del