Canonical Allele Identifier: CA2480872857

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154447498_154447512delinsCACACATATATATAT , CM000663.2:g.154447498_154447512delinsCACACATATATATAT	GRCh38
NC_000001.10:g.154419974_154419988delinsCACACATATATATAT , CM000663.1:g.154419974_154419988delinsCACACATATATATAT	GRCh37
NC_000001.9:g.152686598_152686612delinsCACACATATATATAT	NCBI36
NG_012087.1:g.47306_47320delinsCACACATATATATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.950-627_950-613delinsCACACATATATATAT MANE Select	ENSP00000357470.3:n.950-627_950-613delinsCACACATATATATAT
ENST00000344086.8:c.950-627_950-613delinsCACACATATATATAT	ENSP00000340589.4:n.950-627_950-613delinsCACACATATATATAT
ENST00000368485.7:c.950-627_950-613delinsCACACATATATATAT	ENSP00000357470.3:n.950-627_950-613delinsCACACATATATATAT
ENST00000476006.5:c.766-627_766-613delinsCACACATATATATAT
ENST00000507256.1:n.148-627_148-613delinsCACACATATATATAT
ENST00000515190.1:c.358-627_358-613delinsCACACATATATATAT
NM_000565.3:c.950-627_950-613delinsCACACATATATATAT	NP_000556.1:n.950-627_950-613delinsCACACATATATATAT
NM_181359.2:c.950-627_950-613delinsCACACATATATATAT	NP_852004.1:n.950-627_950-613delinsCACACATATATATAT
XM_005245139.1:c.808-627_808-613delinsCACACATATATATAT	XP_005245196.1:n.808-627_808-613delinsCACACATATATATAT
XM_005245140.1:c.808-627_808-613delinsCACACATATATATAT	XP_005245197.1:n.808-627_808-613delinsCACACATATATATAT
XM_006711298.1:c.998-627_998-613delinsCACACATATATATAT	XP_006711361.1:n.998-627_998-613delinsCACACATATATATAT
XM_006711299.2:c.998-627_998-613delinsCACACATATATATAT	XP_006711362.1:n.998-627_998-613delinsCACACATATATATAT
XM_005245139.2:c.808-627_808-613delinsCACACATATATATAT	XP_005245196.1:n.808-627_808-613delinsCACACATATATATAT
XM_005245140.3:c.808-627_808-613delinsCACACATATATATAT	XP_005245197.1:n.808-627_808-613delinsCACACATATATATAT
XM_006711298.2:c.998-627_998-613delinsCACACATATATATAT	XP_006711361.1:n.998-627_998-613delinsCACACATATATATAT
XM_006711299.4:c.998-627_998-613delinsCACACATATATATAT	XP_006711362.1:n.998-627_998-613delinsCACACATATATATAT
XM_017001199.2:c.998-627_998-613delinsCACACATATATATAT	XP_016856688.1:n.998-627_998-613delinsCACACATATATATAT
XM_017001200.2:c.950-627_950-613delinsCACACATATATATAT	XP_016856689.1:n.950-627_950-613delinsCACACATATATATAT
XM_017001201.2:c.808-627_808-613delinsCACACATATATATAT	XP_016856690.1:n.808-627_808-613delinsCACACATATATATAT
NM_000565.4:c.950-627_950-613delinsCACACATATATATAT MANE Select	NP_000556.1:n.950-627_950-613delinsCACACATATATATAT
NM_181359.3:c.950-627_950-613delinsCACACATATATATAT	NP_852004.1:n.950-627_950-613delinsCACACATATATATAT
NM_001382769.1:c.950-627_950-613delinsCACACATATATATAT	NP_001369698.1:n.950-627_950-613delinsCACACATATATATAT
NM_001382770.1:c.1043-627_1043-613delinsCACACATATATATAT	NP_001369699.1:n.1043-627_1043-613delinsCACACATATATATAT
NM_001382771.1:c.998-627_998-613delinsCACACATATATATAT	NP_001369700.1:n.998-627_998-613delinsCACACATATATATAT
NM_001382772.1:c.944-627_944-613delinsCACACATATATATAT	NP_001369701.1:n.944-627_944-613delinsCACACATATATATAT
NM_001382773.1:c.998-627_998-613delinsCACACATATATATAT	NP_001369702.1:n.998-627_998-613delinsCACACATATATATAT
NM_001382774.1:c.590-627_590-613delinsCACACATATATATAT	NP_001369703.1:n.590-627_590-613delinsCACACATATATATAT