Canonical Allele Identifier: CA505371255

Gene: TYK2

Linked Data

• dbSNP Id: rs2040861264
• MyVariant Identifiers: chr19:g.10463164C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352488C>G , CM000681.2:g.10352488C>G	GRCh38
NC_000019.9:g.10463164C>G , CM000681.1:g.10463164C>G	GRCh37
NC_000019.8:g.10324164C>G	NCBI36
NG_007872.1:g.33085G>C , LRG_121:g.33085G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1613G>C	ENSP00000514307.1:n.*1613G>C
ENST00000525976.6:c.3264G>C	ENSP00000434831.2:p.Gly1088=
ENST00000527481.3:c.*34G>C	ENSP00000466340.2:n.*34G>C
ENST00000529370.6:n.4640G>C
ENST00000529739.2:n.4073G>C
ENST00000530829.2:c.*2815G>C	ENSP00000436826.2:n.*2815G>C
ENST00000531836.6:c.3264G>C	ENSP00000436175.2:p.Gly1088=
ENST00000533334.2:c.*1242+438G>C	ENSP00000432320.2:n.*1242+438G>C
ENST00000534228.2:n.5054+438G>C
ENST00000699354.1:n.1366G>C
ENST00000699355.1:c.*2764G>C	ENSP00000514328.1:n.*2764G>C
ENST00000699356.1:n.4073G>C
ENST00000699357.1:n.5118G>C
ENST00000699358.1:c.3200+438G>C	ENSP00000514329.1:n.3200+438G>C
ENST00000699359.1:c.438G>C
ENST00000699360.1:c.3222G>C	ENSP00000514331.1:p.Gly1074=
ENST00000699361.1:n.298G>C
ENST00000699362.1:c.160G>C	ENSP00000514332.1:n.160G>C
ENST00000699363.1:c.160G>C	ENSP00000514333.1:n.160G>C
ENST00000699364.1:n.264G>C
ENST00000699365.1:c.333G>C	ENSP00000514334.1:p.Gly111=
ENST00000699366.1:n.111+1326G>C
ENST00000699367.1:n.112-1326G>C
ENST00000699368.1:c.751G>C	ENSP00000514335.1:n.751G>C
ENST00000525621.6:c.3264G>C MANE Select	ENSP00000431885.1:p.Gly1088=
ENST00000264818.10:c.3264G>C	ENSP00000264818.6:p.Gly1088=
ENST00000524462.5:c.2709G>C	ENSP00000433203.1:p.Gly903=
ENST00000525621.5:c.3264G>C	ENSP00000431885.1:p.Gly1088=
ENST00000525976.5:c.5G>C
ENST00000527481.2:c.441G>C
ENST00000529422.1:n.116+534G>C
ENST00000529739.1:c.333G>C	ENSP00000436155.1:p.Gly111=
ENST00000530220.1:n.331+438G>C
ENST00000530560.5:c.338-1520G>C	ENSP00000465291.1:n.338-1520G>C
ENST00000592137.1:n.418G>C
NM_003331.4:c.3264G>C , LRG_121t1:c.3264G>C	NP_003322.3:p.Gly1088=
XM_011528245.1:c.3264G>C	XP_011526547.1:p.Gly1088=
XM_011528246.1:c.2967G>C	XP_011526548.1:p.Gly989=
XM_011528247.1:c.2967G>C	XP_011526549.1:p.Gly989=
XM_011528248.1:c.3200+438G>C	XP_011526550.1:n.3200+438G>C
XM_011528249.1:c.1938G>C	XP_011526551.1:p.Gly646=
XM_011528251.1:c.1521G>C	XP_011526553.1:p.Gly507=
XM_011528246.3:c.2967G>C	XP_011526548.1:p.Gly989=
XM_011528249.2:c.1938G>C	XP_011526551.1:p.Gly646=
XR_001753750.1:n.3357+438G>C
XR_001753751.1:n.3816G>C
XR_002958353.1:n.4742G>C
NM_003331.5:c.3264G>C MANE Select	NP_003322.3:p.Gly1088=
NM_001385197.1:c.3264G>C	NP_001372126.1:p.Gly1088=
NM_001385198.1:c.3168+470G>C	NP_001372127.1:n.3168+470G>C
NM_001385199.1:c.3078G>C	NP_001372128.1:p.Gly1026=
NM_001385200.1:c.3261G>C	NP_001372129.1:p.Gly1087=
NM_001385201.1:c.3066G>C	NP_001372130.1:p.Gly1022=
NM_001385202.1:c.3180G>C	NP_001372131.1:p.Gly1060=
NM_001385203.1:c.3345G>C	NP_001372132.1:p.Gly1115=
NM_001385204.1:c.3474G>C	NP_001372133.1:p.Gly1158=
NM_001385205.1:c.3174G>C	NP_001372134.1:p.Gly1058=
NM_001385206.1:c.3138G>C	NP_001372135.1:p.Gly1046=
NM_001385207.1:c.3246G>C	NP_001372136.1:p.Gly1082=