Canonical Allele Identifier: CA403983007

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10463130A>C (hg19) ; chr19:g.10352454A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352454A>C , CM000681.2:g.10352454A>C	GRCh38
NC_000019.9:g.10463130A>C , CM000681.1:g.10463130A>C	GRCh37
NC_000019.8:g.10324130A>C	NCBI36
NG_007872.1:g.33119T>G , LRG_121:g.33119T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000524470.2:c.*1647T>G	ENSP00000514307.1:n.*1647T>G
ENST00000525976.6:c.3298T>G	ENSP00000434831.2:p.Ser1100Ala
ENST00000527481.3:c.*68T>G	ENSP00000466340.2:n.*68T>G
ENST00000529370.6:n.4674T>G
ENST00000529739.2:n.4107T>G
ENST00000530829.2:c.*2849T>G	ENSP00000436826.2:n.*2849T>G
ENST00000531836.6:c.3298T>G	ENSP00000436175.2:p.Ser1100Ala
ENST00000533334.2:c.*1242+472T>G	ENSP00000432320.2:n.*1242+472T>G
ENST00000534228.2:n.5054+472T>G
ENST00000699354.1:n.1400T>G
ENST00000699355.1:c.*2798T>G	ENSP00000514328.1:n.*2798T>G
ENST00000699356.1:n.4107T>G
ENST00000699357.1:n.5152T>G
ENST00000699358.1:c.3200+472T>G	ENSP00000514329.1:n.3200+472T>G
ENST00000699359.1:c.472T>G
ENST00000699360.1:c.3256T>G	ENSP00000514331.1:p.Ser1086Ala
ENST00000699361.1:n.332T>G
ENST00000699362.1:c.194T>G	ENSP00000514332.1:n.194T>G
ENST00000699363.1:c.194T>G	ENSP00000514333.1:n.194T>G
ENST00000699364.1:n.298T>G
ENST00000699365.1:c.367T>G	ENSP00000514334.1:p.Ser123Ala
ENST00000699366.1:n.111+1360T>G
ENST00000699367.1:n.112-1292T>G
ENST00000699368.1:c.785T>G	ENSP00000514335.1:n.785T>G
ENST00000525621.6:c.3298T>G MANE Select	ENSP00000431885.1:p.Ser1100Ala
ENST00000264818.10:c.3298T>G	ENSP00000264818.6:p.Ser1100Ala
ENST00000524462.5:c.2743T>G	ENSP00000433203.1:p.Ser915Ala
ENST00000525621.5:c.3298T>G	ENSP00000431885.1:p.Ser1100Ala
ENST00000525976.5:c.39T>G
ENST00000527481.2:c.475T>G
ENST00000529422.1:n.116+568T>G
ENST00000529739.1:c.367T>G	ENSP00000436155.1:p.Ser123Ala
ENST00000530220.1:n.331+472T>G
ENST00000530560.5:c.338-1486T>G	ENSP00000465291.1:n.338-1486T>G
ENST00000592137.1:n.452T>G
NM_003331.4:c.3298T>G , LRG_121t1:c.3298T>G	NP_003322.3:p.Ser1100Ala
XM_011528245.1:c.3298T>G	XP_011526547.1:p.Ser1100Ala
XM_011528246.1:c.3001T>G	XP_011526548.1:p.Ser1001Ala
XM_011528247.1:c.3001T>G	XP_011526549.1:p.Ser1001Ala
XM_011528248.1:c.3200+472T>G	XP_011526550.1:n.3200+472T>G
XM_011528249.1:c.1972T>G	XP_011526551.1:p.Ser658Ala
XM_011528251.1:c.1555T>G	XP_011526553.1:p.Ser519Ala
XM_011528246.3:c.3001T>G	XP_011526548.1:p.Ser1001Ala
XM_011528249.2:c.1972T>G	XP_011526551.1:p.Ser658Ala
XR_001753750.1:n.3357+472T>G
XR_001753751.1:n.3850T>G
XR_002958353.1:n.4776T>G
NM_003331.5:c.3298T>G MANE Select	NP_003322.3:p.Ser1100Ala
NM_001385197.1:c.3298T>G	NP_001372126.1:p.Ser1100Ala
NM_001385198.1:c.3168+504T>G	NP_001372127.1:n.3168+504T>G
NM_001385199.1:c.3112T>G	NP_001372128.1:p.Ser1038Ala
NM_001385200.1:c.3295T>G	NP_001372129.1:p.Ser1099Ala
NM_001385201.1:c.3100T>G	NP_001372130.1:p.Ser1034Ala
NM_001385202.1:c.3214T>G	NP_001372131.1:p.Ser1072Ala
NM_001385203.1:c.3379T>G	NP_001372132.1:p.Ser1127Ala
NM_001385204.1:c.3508T>G	NP_001372133.1:p.Ser1170Ala
NM_001385205.1:c.3208T>G	NP_001372134.1:p.Ser1070Ala
NM_001385206.1:c.3172T>G	NP_001372135.1:p.Ser1058Ala
NM_001385207.1:c.3280T>G	NP_001372136.1:p.Ser1094Ala