Canonical Allele Identifier: CA646129403

Gene: IL6R

Linked Data

• COSMIC: COSN20090365

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465629_154465630insA , CM000663.2:g.154465629_154465630insA	GRCh38
NC_000001.10:g.154438105_154438106insA , CM000663.1:g.154438105_154438106insA	GRCh37
NC_000001.9:g.152704729_152704730insA	NCBI36
NG_012087.1:g.65437_65438insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.*249_*250insA MANE Select	ENSP00000357470.3:n.*249_*250insA
ENST00000344086.8:c.*464_*465insA	ENSP00000340589.4:n.*464_*465insA
ENST00000368485.7:c.*249_*250insA	ENSP00000357470.3:n.*249_*250insA
NM_000565.3:c.*249_*250insA	NP_000556.1:n.*249_*250insA
NM_181359.2:c.*464_*465insA	NP_852004.1:n.*464_*465insA
XM_005245139.1:c.*337_*338insA	XP_005245196.1:n.*337_*338insA
XM_005245140.1:c.*497_*498insA	XP_005245197.1:n.*497_*498insA
XM_006711298.1:c.*249_*250insA	XP_006711361.1:n.*249_*250insA
XM_005245139.2:c.*337_*338insA	XP_005245196.1:n.*337_*338insA
XM_005245140.3:c.*497_*498insA	XP_005245197.1:n.*497_*498insA
XM_006711298.2:c.*249_*250insA	XP_006711361.1:n.*249_*250insA
XM_017001199.2:c.*249_*250insA	XP_016856688.1:n.*249_*250insA
XM_017001200.2:c.*249_*250insA	XP_016856689.1:n.*249_*250insA
XM_017001201.2:c.*497_*498insA	XP_016856690.1:n.*497_*498insA
NM_000565.4:c.*249_*250insA MANE Select	NP_000556.1:n.*249_*250insA
NM_181359.3:c.*464_*465insA	NP_852004.1:n.*464_*465insA
NM_001382769.1:c.*249_*250insA	NP_001369698.1:n.*249_*250insA
NM_001382770.1:c.*249_*250insA	NP_001369699.1:n.*249_*250insA
NM_001382771.1:c.*249_*250insA	NP_001369700.1:n.*249_*250insA
NM_001382772.1:c.*249_*250insA	NP_001369701.1:n.*249_*250insA
NM_001382773.1:c.*464_*465insA	NP_001369702.1:n.*464_*465insA
NM_001382774.1:c.*249_*250insA	NP_001369703.1:n.*249_*250insA