Canonical Allele Identifier: CA403983344

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10463220G>C (hg19) ; chr19:g.10352544G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352544G>C , CM000681.2:g.10352544G>C	GRCh38
NC_000019.9:g.10463220G>C , CM000681.1:g.10463220G>C	GRCh37
NC_000019.8:g.10324220G>C	NCBI36
NG_007872.1:g.33029C>G , LRG_121:g.33029C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1557C>G	ENSP00000514307.1:n.*1557C>G
ENST00000525976.6:c.3208C>G	ENSP00000434831.2:p.Pro1070Ala
ENST00000527481.3:c.3089C>G	ENSP00000466340.2:p.Pro1030Arg
ENST00000529370.6:n.4584C>G
ENST00000529739.2:n.4017C>G
ENST00000530829.2:c.*2759C>G	ENSP00000436826.2:n.*2759C>G
ENST00000531836.6:c.3208C>G	ENSP00000436175.2:p.Pro1070Ala
ENST00000533334.2:c.*1242+382C>G	ENSP00000432320.2:n.*1242+382C>G
ENST00000534228.2:n.5054+382C>G
ENST00000699354.1:n.1310C>G
ENST00000699355.1:c.*2708C>G	ENSP00000514328.1:n.*2708C>G
ENST00000699356.1:n.4017C>G
ENST00000699357.1:n.5062C>G
ENST00000699358.1:c.3200+382C>G	ENSP00000514329.1:n.3200+382C>G
ENST00000699359.1:c.382C>G
ENST00000699360.1:c.3166C>G	ENSP00000514331.1:p.Pro1056Ala
ENST00000699361.1:n.242C>G
ENST00000699362.1:c.104C>G	ENSP00000514332.1:p.Pro35Arg
ENST00000699363.1:c.104C>G	ENSP00000514333.1:p.Pro35Arg
ENST00000699364.1:n.208C>G
ENST00000699365.1:c.277C>G	ENSP00000514334.1:p.Pro93Ala
ENST00000699366.1:n.111+1270C>G
ENST00000699367.1:n.111+1270C>G
ENST00000699368.1:c.695C>G	ENSP00000514335.1:n.695C>G
ENST00000525621.6:c.3208C>G MANE Select	ENSP00000431885.1:p.Pro1070Ala
ENST00000264818.10:c.3208C>G	ENSP00000264818.6:p.Pro1070Ala
ENST00000524462.5:c.2653C>G	ENSP00000433203.1:p.Pro885Ala
ENST00000525621.5:c.3208C>G	ENSP00000431885.1:p.Pro1070Ala
ENST00000527481.2:c.385C>G
ENST00000529422.1:n.116+478C>G
ENST00000529739.1:c.277C>G	ENSP00000436155.1:p.Pro93Ala
ENST00000530220.1:n.331+382C>G
ENST00000530560.5:c.337+1498C>G	ENSP00000465291.1:n.337+1498C>G
ENST00000592137.1:n.362C>G
NM_003331.4:c.3208C>G , LRG_121t1:c.3208C>G	NP_003322.3:p.Pro1070Ala
XM_011528245.1:c.3208C>G	XP_011526547.1:p.Pro1070Ala
XM_011528246.1:c.2911C>G	XP_011526548.1:p.Pro971Ala
XM_011528247.1:c.2911C>G	XP_011526549.1:p.Pro971Ala
XM_011528248.1:c.3200+382C>G	XP_011526550.1:n.3200+382C>G
XM_011528249.1:c.1882C>G	XP_011526551.1:p.Pro628Ala
XM_011528251.1:c.1465C>G	XP_011526553.1:p.Pro489Ala
XM_011528246.3:c.2911C>G	XP_011526548.1:p.Pro971Ala
XM_011528249.2:c.1882C>G	XP_011526551.1:p.Pro628Ala
XR_001753750.1:n.3357+382C>G
XR_001753751.1:n.3760C>G
XR_002958353.1:n.4686C>G
NM_003331.5:c.3208C>G MANE Select	NP_003322.3:p.Pro1070Ala
NM_001385197.1:c.3208C>G	NP_001372126.1:p.Pro1070Ala
NM_001385198.1:c.3168+414C>G	NP_001372127.1:n.3168+414C>G
NM_001385199.1:c.3022C>G	NP_001372128.1:p.Pro1008Ala
NM_001385200.1:c.3205C>G	NP_001372129.1:p.Pro1069Ala
NM_001385201.1:c.3010C>G	NP_001372130.1:p.Pro1004Ala
NM_001385202.1:c.3124C>G	NP_001372131.1:p.Pro1042Ala
NM_001385203.1:c.3289C>G	NP_001372132.1:p.Pro1097Ala
NM_001385204.1:c.3418C>G	NP_001372133.1:p.Pro1140Ala
NM_001385205.1:c.3118C>G	NP_001372134.1:p.Pro1040Ala
NM_001385206.1:c.3082C>G	NP_001372135.1:p.Pro1028Ala
NM_001385207.1:c.3190C>G	NP_001372136.1:p.Pro1064Ala