Canonical Allele Identifier: CA2480880332

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465319_154465320delinsAT , CM000663.2:g.154465319_154465320delinsAT	GRCh38
NC_000001.10:g.154437795_154437796delinsAT , CM000663.1:g.154437795_154437796delinsAT	GRCh37
NC_000001.9:g.152704419_152704420delinsAT	NCBI36
NG_012087.1:g.65127_65128delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1346_1347delinsAT MANE Select	ENSP00000357470.3:p.Asp449=
ENST00000344086.8:c.*154_*155delinsAT	ENSP00000340589.4:n.*154_*155delinsAT
ENST00000368485.7:c.1346_1347delinsAT	ENSP00000357470.3:p.Asp449=
NM_000565.3:c.1346_1347delinsAT	NP_000556.1:p.Asp449=
NM_181359.2:c.*154_*155delinsAT	NP_852004.1:n.*154_*155delinsAT
XM_005245139.1:c.*27_*28delinsAT	XP_005245196.1:n.*27_*28delinsAT
XM_005245140.1:c.*187_*188delinsAT	XP_005245197.1:n.*187_*188delinsAT
XM_006711298.1:c.1394_1395delinsAT	XP_006711361.1:p.Asp465=
XM_005245139.2:c.*27_*28delinsAT	XP_005245196.1:n.*27_*28delinsAT
XM_005245140.3:c.*187_*188delinsAT	XP_005245197.1:n.*187_*188delinsAT
XM_006711298.2:c.1394_1395delinsAT	XP_006711361.1:p.Asp465=
XM_017001199.2:c.1493_1494delinsAT	XP_016856688.1:p.Asp498=
XM_017001200.2:c.1445_1446delinsAT	XP_016856689.1:p.Asp482=
XM_017001201.2:c.*187_*188delinsAT	XP_016856690.1:n.*187_*188delinsAT
NM_000565.4:c.1346_1347delinsAT MANE Select	NP_000556.1:p.Asp449=
NM_181359.3:c.*154_*155delinsAT	NP_852004.1:n.*154_*155delinsAT
NM_001382769.1:c.1445_1446delinsAT	NP_001369698.1:p.Asp482=
NM_001382770.1:c.1439_1440delinsAT	NP_001369699.1:p.Asp480=
NM_001382771.1:c.1394_1395delinsAT	NP_001369700.1:p.Asp465=
NM_001382772.1:c.1340_1341delinsAT	NP_001369701.1:p.Asp447=
NM_001382773.1:c.*154_*155delinsAT	NP_001369702.1:n.*154_*155delinsAT
NM_001382774.1:c.986_987delinsAT	NP_001369703.1:p.Asp329=