Canonical Allele Identifier: CA2746185967

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154454288_154454289insGAAA , CM000663.2:g.154454288_154454289insGAAA	GRCh38
NC_000001.10:g.154426764_154426765insGAAA , CM000663.1:g.154426764_154426765insGAAA	GRCh37
NC_000001.9:g.152693388_152693389insGAAA	NCBI36
NG_012087.1:g.54096_54097insGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1067-200_1067-199insGAAA MANE Select	ENSP00000357470.3:n.1067-200_1067-199insGAAA
ENST00000344086.8:c.1066+4308_1066+4309insGAAA	ENSP00000340589.4:n.1066+4308_1066+4309insGAAA
ENST00000368485.7:c.1067-200_1067-199insGAAA	ENSP00000357470.3:n.1067-200_1067-199insGAAA
ENST00000502679.1:n.180_181insGAAA
ENST00000507256.1:n.265-200_265-199insGAAA
ENST00000515190.1:c.475-200_475-199insGAAA
NM_000565.3:c.1067-200_1067-199insGAAA	NP_000556.1:n.1067-200_1067-199insGAAA
NM_181359.2:c.1066+4308_1066+4309insGAAA	NP_852004.1:n.1066+4308_1066+4309insGAAA
XM_005245139.1:c.924+4308_924+4309insGAAA	XP_005245196.1:n.924+4308_924+4309insGAAA
XM_005245140.1:c.925-200_925-199insGAAA	XP_005245197.1:n.925-200_925-199insGAAA
XM_006711298.1:c.1115-200_1115-199insGAAA	XP_006711361.1:n.1115-200_1115-199insGAAA
XM_006711299.2:c.1114+4308_1114+4309insGAAA	XP_006711362.1:n.1114+4308_1114+4309insGAAA
XM_005245139.2:c.924+4308_924+4309insGAAA	XP_005245196.1:n.924+4308_924+4309insGAAA
XM_005245140.3:c.925-200_925-199insGAAA	XP_005245197.1:n.925-200_925-199insGAAA
XM_006711298.2:c.1115-200_1115-199insGAAA	XP_006711361.1:n.1115-200_1115-199insGAAA
XM_006711299.4:c.1114+4308_1114+4309insGAAA	XP_006711362.1:n.1114+4308_1114+4309insGAAA
XM_017001199.2:c.1213+117_1213+118insGAAA	XP_016856688.1:n.1213+117_1213+118insGAAA
XM_017001200.2:c.1165+117_1165+118insGAAA	XP_016856689.1:n.1165+117_1165+118insGAAA
XM_017001201.2:c.1023+117_1023+118insGAAA	XP_016856690.1:n.1023+117_1023+118insGAAA
NM_000565.4:c.1067-200_1067-199insGAAA MANE Select	NP_000556.1:n.1067-200_1067-199insGAAA
NM_181359.3:c.1066+4308_1066+4309insGAAA	NP_852004.1:n.1066+4308_1066+4309insGAAA
NM_001382769.1:c.1165+117_1165+118insGAAA	NP_001369698.1:n.1165+117_1165+118insGAAA
NM_001382770.1:c.1160-200_1160-199insGAAA	NP_001369699.1:n.1160-200_1160-199insGAAA
NM_001382771.1:c.1115-200_1115-199insGAAA	NP_001369700.1:n.1115-200_1115-199insGAAA
NM_001382772.1:c.1061-200_1061-199insGAAA	NP_001369701.1:n.1061-200_1061-199insGAAA
NM_001382773.1:c.1114+4308_1114+4309insGAAA	NP_001369702.1:n.1114+4308_1114+4309insGAAA
NM_001382774.1:c.707-200_707-199insGAAA	NP_001369703.1:n.707-200_707-199insGAAA