Canonical Allele Identifier: CA952281780

Gene: KSR2

Linked Data

• dbSNP Id: rs1874842780

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117522725_117522726insTCAAAGACACACCAGCTCTTCTCTGAGCCCACAGCATCTGTTCTGGGCCTGGTAAGATGCAAGACTTGTGCATTTGGGGTCT , CM000674.2:g.117522725_117522726insTCAAAGACACACCAGCTCTTCTCTGAGCCCACAGCATCTGTTCTGGGCCTGGTAAGATGCAAGACTTGTGCATTTGGGGTCT	GRCh38
NC_000012.11:g.117960530_117960531insTCAAAGACACACCAGCTCTTCTCTGAGCCCACAGCATCTGTTCTGGGCCTGGTAAGATGCAAGACTTGTGCATTTGGGGTCT , CM000674.1:g.117960530_117960531insTCAAAGACACACCAGCTCTTCTCTGAGCCCACAGCATCTGTTCTGGGCCTGGTAAGATGCAAGACTTGTGCATTTGGGGTCT	GRCh37
NC_000012.10:g.116444913_116444914insTCAAAGACACACCAGCTCTTCTCTGAGCCCACAGCATCTGTTCTGGGCCTGGTAAGATGCAAGACTTGTGCATTTGGGGTCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339824.7:c.2219+2126_2219+2127insAGACCCCAAATGCACAAGTCTTGCATCTTACCAGGCCCAGAACAGATGCTGTGGGCTCAGAGAAGAGCTGGTGTGTCTTTGA MANE Select	ENSP00000339952.4:n.2219+2126_2219+2127insAGACCCCAAATGCACAAGT...
ENST00000339824.6:c.2219+2126_2219+2127insAGACCCCAAATGCACAAGTCTTGCATCTTACCAGGCCCAGAACAGATGCTGTGGGCTCAGAGAAGAGCTGGTGTGTCTTTGA	ENSP00000339952.4:n.2219+2126_2219+2127insAGACCCCAAATGCACAAGT...
ENST00000425217.5:c.2132+2126_2132+2127insAGACCCCAAATGCACAAGTCTTGCATCTTACCAGGCCCAGAACAGATGCTGTGGGCTCAGAGAAGAGCTGGTGTGTCTTTGA	ENSP00000389715.1:n.2132+2126_2132+2127insAGACCCCAAATGCACAAGT...
ENST00000545002.1:n.1365+2126_1365+2127insAGACCCCAAATGCACAAGTCTTGCATCTTACCAGGCCCAGAACAGATGCTGTGGGCTCAGAGAAGAGCTGGTGTGTCTTTGA
NM_173598.4:c.2132+2126_2132+2127insAGACCCCAAATGCACAAGTCTTGCATCTTACCAGGCCCAGAACAGATGCTGTGGGCTCAGAGAAGAGCTGGTGTGTCTTTGA	NP_775869.3:n.2132+2126_2132+2127insAGACCCCAAATGCACAAGTCTTGCA...
XM_011538224.1:c.2213+2126_2213+2127insAGACCCCAAATGCACAAGTCTTGCATCTTACCAGGCCCAGAACAGATGCTGTGGGCTCAGAGAAGAGCTGGTGTGTCTTTGA	XP_011536526.1:n.2213+2126_2213+2127insAGACCCCAAATGCACAAGTCTT...
XM_011538225.1:c.1856+2126_1856+2127insAGACCCCAAATGCACAAGTCTTGCATCTTACCAGGCCCAGAACAGATGCTGTGGGCTCAGAGAAGAGCTGGTGTGTCTTTGA	XP_011536527.1:n.1856+2126_1856+2127insAGACCCCAAATGCACAAGTCTT...
XM_011538226.1:c.2219+2126_2219+2127insAGACCCCAAATGCACAAGTCTTGCATCTTACCAGGCCCAGAACAGATGCTGTGGGCTCAGAGAAGAGCTGGTGTGTCTTTGA	XP_011536528.1:n.2219+2126_2219+2127insAGACCCCAAATGCACAAGTCTT...
XM_011538227.1:c.1355+2126_1355+2127insAGACCCCAAATGCACAAGTCTTGCATCTTACCAGGCCCAGAACAGATGCTGTGGGCTCAGAGAAGAGCTGGTGTGTCTTTGA	XP_011536529.1:n.1355+2126_1355+2127insAGACCCCAAATGCACAAGTCTT...
XM_011538228.1:c.1310+2126_1310+2127insAGACCCCAAATGCACAAGTCTTGCATCTTACCAGGCCCAGAACAGATGCTGTGGGCTCAGAGAAGAGCTGGTGTGTCTTTGA	XP_011536530.1:n.1310+2126_1310+2127insAGACCCCAAATGCACAAGTCTT...
XM_011538230.1:c.959+2126_959+2127insAGACCCCAAATGCACAAGTCTTGCATCTTACCAGGCCCAGAACAGATGCTGTGGGCTCAGAGAAGAGCTGGTGTGTCTTTGA	XP_011536532.1:n.959+2126_959+2127insAGACCCCAAATGCACAAGTCTTGC...
XR_944522.1:n.3053+2126_3053+2127insAGACCCCAAATGCACAAGTCTTGCATCTTACCAGGCCCAGAACAGATGCTGTGGGCTCAGAGAAGAGCTGGTGTGTCTTTGA
XM_011538224.3:c.2213+2126_2213+2127insAGACCCCAAATGCACAAGTCTTGCATCTTACCAGGCCCAGAACAGATGCTGTGGGCTCAGAGAAGAGCTGGTGTGTCTTTGA	XP_011536526.1:n.2213+2126_2213+2127insAGACCCCAAATGCACAAGTCTT...
XM_011538225.3:c.1856+2126_1856+2127insAGACCCCAAATGCACAAGTCTTGCATCTTACCAGGCCCAGAACAGATGCTGTGGGCTCAGAGAAGAGCTGGTGTGTCTTTGA	XP_011536527.1:n.1856+2126_1856+2127insAGACCCCAAATGCACAAGTCTT...
XM_011538226.3:c.2219+2126_2219+2127insAGACCCCAAATGCACAAGTCTTGCATCTTACCAGGCCCAGAACAGATGCTGTGGGCTCAGAGAAGAGCTGGTGTGTCTTTGA	XP_011536528.1:n.2219+2126_2219+2127insAGACCCCAAATGCACAAGTCTT...
XM_017019208.2:c.2219+2126_2219+2127insAGACCCCAAATGCACAAGTCTTGCATCTTACCAGGCCCAGAACAGATGCTGTGGGCTCAGAGAAGAGCTGGTGTGTCTTTGA	XP_016874697.1:n.2219+2126_2219+2127insAGACCCCAAATGCACAAGTCTT...
XM_017019210.2:c.914+2126_914+2127insAGACCCCAAATGCACAAGTCTTGCATCTTACCAGGCCCAGAACAGATGCTGTGGGCTCAGAGAAGAGCTGGTGTGTCTTTGA	XP_016874699.1:n.914+2126_914+2127insAGACCCCAAATGCACAAGTCTTGC...
NM_173598.6:c.2219+2126_2219+2127insAGACCCCAAATGCACAAGTCTTGCATCTTACCAGGCCCAGAACAGATGCTGTGGGCTCAGAGAAGAGCTGGTGTGTCTTTGA MANE Select	NP_775869.4:n.2219+2126_2219+2127insAGACCCCAAATGCACAAGTCTTGCA...