Canonical Allele Identifier: CA359779504

Gene: IL6ST

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55941692T>G , CM000667.2:g.55941692T>G	GRCh38
NC_000005.9:g.55237520T>G , CM000667.1:g.55237520T>G	GRCh37
NC_000005.8:g.55273277T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002184.4:c.2147A>C MANE Select	NP_002175.2:p.Lys716Thr
ENST00000381298.7:c.2147A>C MANE Select	ENSP00000370698.2:p.Lys716Thr
NM_001190981.1:c.1964A>C	NP_001177910.1:p.Lys655Thr
NM_001190981.2:c.1964A>C	NP_001177910.1:p.Lys655Thr
NM_001364275.1:c.2045A>C	NP_001351204.1:p.Lys682Thr
NM_001364275.2:c.2045A>C	NP_001351204.1:p.Lys682Thr
NM_001364276.1:c.1937A>C	NP_001351205.1:p.Lys646Thr
NM_001364276.2:c.1937A>C	NP_001351205.1:p.Lys646Thr
NM_001364277.1:c.1280A>C	NP_001351206.1:p.Lys427Thr
NM_001364277.2:c.1280A>C	NP_001351206.1:p.Lys427Thr
NM_001364278.1:c.1244A>C	NP_001351207.1:p.Lys415Thr
NM_001364278.2:c.1244A>C	NP_001351207.1:p.Lys415Thr
NM_001364279.1:c.1151A>C	NP_001351208.1:p.Lys384Thr
NM_001364279.2:c.1151A>C	NP_001351208.1:p.Lys384Thr
NM_002184.3:c.2147A>C	NP_002175.2:p.Lys716Thr
NM_175767.2:c.*1074A>C	NP_786943.1:n.*1074A>C
NM_175767.3:c.*1074A>C	NP_786943.1:n.*1074A>C
NR_120480.1:n.2506A>C
NR_120480.2:n.2476A>C
NR_157112.1:n.3311A>C
NR_157112.2:n.3311A>C
ENST00000336909.9:c.2147A>C	ENSP00000338799.5:p.Lys716Thr
ENST00000381287.8:c.*1074A>C	ENSP00000370687.4:n.*1074A>C
ENST00000381294.7:c.1964A>C	ENSP00000370694.3:p.Lys655Thr
ENST00000381294.8:c.1964A>C	ENSP00000370694.3:p.Lys655Thr
ENST00000381298.6:c.2147A>C	ENSP00000370698.2:p.Lys716Thr
ENST00000502326.7:c.2147A>C	ENSP00000462158.1:p.Lys716Thr
ENST00000503773.6:c.*1191A>C	ENSP00000426224.2:n.*1191A>C
ENST00000506241.2:n.3488A>C
ENST00000523039.5:n.312A>C
ENST00000577363.2:c.*1552A>C	ENSP00000513861.1:n.*1552A>C
ENST00000651614.1:c.*1099A>C	ENSP00000498224.1:n.*1099A>C
ENST00000698638.1:c.1244A>C	ENSP00000513851.1:p.Lys415Thr
ENST00000698639.1:c.2000A>C	ENSP00000513852.1:p.Lys667Thr
ENST00000698640.1:c.1430A>C	ENSP00000513853.1:n.1430A>C
ENST00000698641.1:c.*1369A>C	ENSP00000513854.1:n.*1369A>C
ENST00000698642.1:c.*1598A>C	ENSP00000513855.1:n.*1598A>C
ENST00000698643.1:c.*1469A>C	ENSP00000513856.1:n.*1469A>C
ENST00000698644.1:c.1937A>C	ENSP00000513857.1:p.Lys646Thr
ENST00000698645.1:c.2147A>C	ENSP00000513858.1:p.Lys716Thr
ENST00000698646.1:c.2045A>C	ENSP00000513859.1:p.Lys682Thr
ENST00000698647.1:c.*1766A>C	ENSP00000513860.1:n.*1766A>C
ENST00000698648.1:c.*1552A>C	ENSP00000513862.1:n.*1552A>C
ENST00000698649.1:n.1149A>C