Canonical Allele Identifier: CA2582370046

Gene: TYK2

Linked Data

• gnomAD v4: 19-10352442-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352442_10352443insC , CM000681.2:g.10352442_10352443insC	GRCh38
NC_000019.9:g.10463118_10463119insC , CM000681.1:g.10463118_10463119insC	GRCh37
NC_000019.8:g.10324118_10324119insC	NCBI36
NG_007872.1:g.33130_33131insG , LRG_121:g.33130_33131insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000524470.2:c.*1658_*1659insG	ENSP00000514307.1:n.*1658_*1659insG
ENST00000525976.6:c.3309_3310insG	ENSP00000434831.2:p.Pro1104AlafsTer?
ENST00000527481.3:c.*79_*80insG	ENSP00000466340.2:n.*79_*80insG
ENST00000529370.6:n.4685_4686insG
ENST00000529739.2:n.4118_4119insG
ENST00000530829.2:c.*2860_*2861insG	ENSP00000436826.2:n.*2860_*2861insG
ENST00000531836.6:c.3309_3310insG	ENSP00000436175.2:p.Pro1104AlafsTer7
ENST00000533334.2:c.*1242+483_*1242+484insG	ENSP00000432320.2:n.*1242+483_*1242+484in...
ENST00000534228.2:n.5054+483_5054+484insG
ENST00000699354.1:n.1411_1412insG
ENST00000699355.1:c.*2809_*2810insG	ENSP00000514328.1:n.*2809_*2810insG
ENST00000699356.1:n.4118_4119insG
ENST00000699357.1:n.5163_5164insG
ENST00000699358.1:c.3200+483_3200+484insG	ENSP00000514329.1:n.3200+483_3200+484insG...
ENST00000699359.1:c.483_484insG
ENST00000699360.1:c.3267_3268insG	ENSP00000514331.1:p.Pro1090AlafsTer7
ENST00000699361.1:n.343_344insG
ENST00000699362.1:c.205_206insG	ENSP00000514332.1:n.205_206insG
ENST00000699363.1:c.205_206insG	ENSP00000514333.1:n.205_206insG
ENST00000699364.1:n.309_310insG
ENST00000699365.1:c.378_379insG	ENSP00000514334.1:p.Pro127AlafsTer7
ENST00000699366.1:n.111+1371_111+1372insG
ENST00000699367.1:n.112-1281_112-1280insG
ENST00000699368.1:c.796_797insG	ENSP00000514335.1:n.796_797insG
ENST00000525621.6:c.3309_3310insG MANE Select	ENSP00000431885.1:p.Pro1104AlafsTer7
ENST00000264818.10:c.3309_3310insG	ENSP00000264818.6:p.Pro1104AlafsTer7
ENST00000524462.5:c.2754_2755insG	ENSP00000433203.1:p.Pro919AlafsTer7
ENST00000525621.5:c.3309_3310insG	ENSP00000431885.1:p.Pro1104AlafsTer7
ENST00000525976.5:c.50_51insG
ENST00000527481.2:c.486_487insG
ENST00000529422.1:n.116+579_116+580insG
ENST00000529739.1:c.378_379insG	ENSP00000436155.1:p.Pro127AlafsTer?
ENST00000530220.1:n.331+483_331+484insG
ENST00000530560.5:c.338-1475_338-1474insG	ENSP00000465291.1:n.338-1475_338-1474insG...
ENST00000592137.1:n.463_464insG
NM_003331.4:c.3309_3310insG , LRG_121t1:c.3309_3310insG	NP_003322.3:p.Pro1104AlafsTer7
XM_011528245.1:c.3309_3310insG	XP_011526547.1:p.Pro1104AlafsTer7
XM_011528246.1:c.3012_3013insG	XP_011526548.1:p.Pro1005AlafsTer7
XM_011528247.1:c.3012_3013insG	XP_011526549.1:p.Pro1005AlafsTer7
XM_011528248.1:c.3200+483_3200+484insG	XP_011526550.1:n.3200+483_3200+484insG
XM_011528249.1:c.1983_1984insG	XP_011526551.1:p.Pro662AlafsTer7
XM_011528251.1:c.1566_1567insG	XP_011526553.1:p.Pro523AlafsTer7
XM_011528246.3:c.3012_3013insG	XP_011526548.1:p.Pro1005AlafsTer7
XM_011528249.2:c.1983_1984insG	XP_011526551.1:p.Pro662AlafsTer7
XR_001753750.1:n.3357+483_3357+484insG
XR_001753751.1:n.3861_3862insG
XR_002958353.1:n.4787_4788insG
NM_003331.5:c.3309_3310insG MANE Select	NP_003322.3:p.Pro1104AlafsTer7
NM_001385197.1:c.3309_3310insG	NP_001372126.1:p.Pro1104AlafsTer?
NM_001385198.1:c.3168+515_3168+516insG	NP_001372127.1:n.3168+515_3168+516insG
NM_001385199.1:c.3123_3124insG	NP_001372128.1:p.Pro1042AlafsTer7
NM_001385200.1:c.3306_3307insG	NP_001372129.1:p.Pro1103AlafsTer7
NM_001385201.1:c.3111_3112insG	NP_001372130.1:p.Pro1038AlafsTer7
NM_001385202.1:c.3225_3226insG	NP_001372131.1:p.Pro1076AlafsTer7
NM_001385203.1:c.3390_3391insG	NP_001372132.1:p.Pro1131AlafsTer7
NM_001385204.1:c.3519_3520insG	NP_001372133.1:p.Pro1174AlafsTer7
NM_001385205.1:c.3219_3220insG	NP_001372134.1:p.Pro1074AlafsTer7
NM_001385206.1:c.3183_3184insG	NP_001372135.1:p.Pro1062AlafsTer7
NM_001385207.1:c.3291_3292insG	NP_001372136.1:p.Pro1098AlafsTer7