Canonical Allele Identifier: CA2480880345

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465360_154465361delinsGA , CM000663.2:g.154465360_154465361delinsGA	GRCh38
NC_000001.10:g.154437836_154437837delinsGA , CM000663.1:g.154437836_154437837delinsGA	GRCh37
NC_000001.9:g.152704460_152704461delinsGA	NCBI36
NG_012087.1:g.65168_65169delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1387_1388delinsGA MANE Select	ENSP00000357470.3:p.Asp463=
ENST00000344086.8:c.*195_*196delinsGA	ENSP00000340589.4:n.*195_*196delinsGA
ENST00000368485.7:c.1387_1388delinsGA	ENSP00000357470.3:p.Asp463=
NM_000565.3:c.1387_1388delinsGA	NP_000556.1:p.Asp463=
NM_181359.2:c.*195_*196delinsGA	NP_852004.1:n.*195_*196delinsGA
XM_005245139.1:c.*68_*69delinsGA	XP_005245196.1:n.*68_*69delinsGA
XM_005245140.1:c.*228_*229delinsGA	XP_005245197.1:n.*228_*229delinsGA
XM_006711298.1:c.1435_1436delinsGA	XP_006711361.1:p.Asp479=
XM_005245139.2:c.*68_*69delinsGA	XP_005245196.1:n.*68_*69delinsGA
XM_005245140.3:c.*228_*229delinsGA	XP_005245197.1:n.*228_*229delinsGA
XM_006711298.2:c.1435_1436delinsGA	XP_006711361.1:p.Asp479=
XM_017001199.2:c.1534_1535delinsGA	XP_016856688.1:p.Asp512=
XM_017001200.2:c.1486_1487delinsGA	XP_016856689.1:p.Asp496=
XM_017001201.2:c.*228_*229delinsGA	XP_016856690.1:n.*228_*229delinsGA
NM_000565.4:c.1387_1388delinsGA MANE Select	NP_000556.1:p.Asp463=
NM_181359.3:c.*195_*196delinsGA	NP_852004.1:n.*195_*196delinsGA
NM_001382769.1:c.1486_1487delinsGA	NP_001369698.1:p.Asp496=
NM_001382770.1:c.1480_1481delinsGA	NP_001369699.1:p.Asp494=
NM_001382771.1:c.1435_1436delinsGA	NP_001369700.1:p.Asp479=
NM_001382772.1:c.1381_1382delinsGA	NP_001369701.1:p.Asp461=
NM_001382773.1:c.*195_*196delinsGA	NP_001369702.1:n.*195_*196delinsGA
NM_001382774.1:c.1027_1028delinsGA	NP_001369703.1:p.Asp343=