Canonical Allele Identifier: CA2682013564

Gene: IL6 STEAP1B IL6-AS1

Linked Data

• gnomAD v4: 7-22727320-GCGGTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22727321_22727325del , CM000669.2:g.22727321_22727325del	GRCh38
NC_000007.13:g.22766940_22766944del , CM000669.1:g.22766940_22766944del	GRCh37
NC_000007.12:g.22733465_22733469del	NCBI36
NG_011640.1:g.5175_5179del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464710.2:n.145_149del (IL6)
ENST00000258743.10:c.19+40_19+44del (IL6) MANE Select	ENSP00000258743.5:n.19+40_19+44del
ENST00000650428.1:n.46+243_46+247del (STEAP1B)
ENST00000258743.9:c.19+40_19+44del (IL6)	ENSP00000258743.5:n.19+40_19+44del
ENST00000401630.7:c.19+40_19+44del (IL6)	ENSP00000384928.3:n.19+40_19+44del
ENST00000401651.5:c.-19+40_-19+44del (IL6)	ENSP00000385718.1:n.-19+40_-19+44del
ENST00000404625.5:c.19+40_19+44del (IL6)	ENSP00000385675.1:n.19+40_19+44del
ENST00000406575.1:c.19+40_19+44del (IL6)	ENSP00000385227.1:n.19+40_19+44del
ENST00000407492.5:c.-19+40_-19+44del (IL6)	ENSP00000385043.1:n.-19+40_-19+44del
ENST00000426291.5:c.19+40_19+44del (IL6)	ENSP00000405150.1:n.19+40_19+44del
ENST00000485300.1:n.122_126del (IL6)
NM_000600.3:c.19+40_19+44del (IL6)	NP_000591.1:n.19+40_19+44del
NR_131935.1:n.53+243_53+247del (IL6-AS1)
XM_005249745.3:c.59_63del (IL6)	XP_005249802.1:p.Ala20GlyfsTer?
XM_011515390.1:c.19+40_19+44del (IL6)	XP_011513692.1:n.19+40_19+44del
XM_011515391.1:c.-19+40_-19+44del (IL6)	XP_011513693.1:n.-19+40_-19+44del
NM_000600.4:c.19+40_19+44del (IL6)	NP_000591.1:n.19+40_19+44del
NM_001318095.1:c.-19+40_-19+44del (IL6)	NP_001305024.1:n.-19+40_-19+44del
XM_005249745.5:c.59_63del (IL6)	XP_005249802.1:p.Ala20GlyfsTer?
XM_011515390.2:c.19+40_19+44del (IL6)	XP_011513692.1:n.19+40_19+44del
NM_000600.5:c.19+40_19+44del (IL6) MANE Select	NP_000591.1:n.19+40_19+44del
NM_001318095.2:c.-19+40_-19+44del (IL6)	NP_001305024.1:n.-19+40_-19+44del
NM_001371096.1:c.19+40_19+44del (IL6)	NP_001358025.1:n.19+40_19+44del