Canonical Allele Identifier: CA2480880504

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465777_154465782delinsATTTCC , CM000663.2:g.154465777_154465782delinsATTTCC	GRCh38
NC_000001.10:g.154438253_154438258delinsATTTCC , CM000663.1:g.154438253_154438258delinsATTTCC	GRCh37
NC_000001.9:g.152704877_152704882delinsATTTCC	NCBI36
NG_012087.1:g.65585_65590delinsATTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.*397_*402delinsATTTCC MANE Select	ENSP00000357470.3:n.*397_*402delinsATTTCC
ENST00000344086.8:c.*612_*617delinsATTTCC	ENSP00000340589.4:n.*612_*617delinsATTTCC
ENST00000368485.7:c.*397_*402delinsATTTCC	ENSP00000357470.3:n.*397_*402delinsATTTCC
NM_000565.3:c.*397_*402delinsATTTCC	NP_000556.1:n.*397_*402delinsATTTCC
NM_181359.2:c.*612_*617delinsATTTCC	NP_852004.1:n.*612_*617delinsATTTCC
XM_005245139.1:c.*485_*490delinsATTTCC	XP_005245196.1:n.*485_*490delinsATTTCC
XM_005245140.1:c.*645_*650delinsATTTCC	XP_005245197.1:n.*645_*650delinsATTTCC
XM_006711298.1:c.*397_*402delinsATTTCC	XP_006711361.1:n.*397_*402delinsATTTCC
XM_005245139.2:c.*485_*490delinsATTTCC	XP_005245196.1:n.*485_*490delinsATTTCC
XM_005245140.3:c.*645_*650delinsATTTCC	XP_005245197.1:n.*645_*650delinsATTTCC
XM_006711298.2:c.*397_*402delinsATTTCC	XP_006711361.1:n.*397_*402delinsATTTCC
XM_017001199.2:c.*397_*402delinsATTTCC	XP_016856688.1:n.*397_*402delinsATTTCC
XM_017001200.2:c.*397_*402delinsATTTCC	XP_016856689.1:n.*397_*402delinsATTTCC
XM_017001201.2:c.*645_*650delinsATTTCC	XP_016856690.1:n.*645_*650delinsATTTCC
NM_000565.4:c.*397_*402delinsATTTCC MANE Select	NP_000556.1:n.*397_*402delinsATTTCC
NM_181359.3:c.*612_*617delinsATTTCC	NP_852004.1:n.*612_*617delinsATTTCC
NM_001382769.1:c.*397_*402delinsATTTCC	NP_001369698.1:n.*397_*402delinsATTTCC
NM_001382770.1:c.*397_*402delinsATTTCC	NP_001369699.1:n.*397_*402delinsATTTCC
NM_001382771.1:c.*397_*402delinsATTTCC	NP_001369700.1:n.*397_*402delinsATTTCC
NM_001382772.1:c.*397_*402delinsATTTCC	NP_001369701.1:n.*397_*402delinsATTTCC
NM_001382773.1:c.*612_*617delinsATTTCC	NP_001369702.1:n.*612_*617delinsATTTCC
NM_001382774.1:c.*397_*402delinsATTTCC	NP_001369703.1:n.*397_*402delinsATTTCC