Canonical Allele Identifier: CA920056973

Gene: TYK2

Linked Data

• dbSNP Id: rs1568327325

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10353979_10353986del , CM000681.2:g.10353979_10353986del	GRCh38
NC_000019.9:g.10464655_10464662del , CM000681.1:g.10464655_10464662del	GRCh37
NC_000019.8:g.10325655_10325662del	NCBI36
NG_007872.1:g.31592_31599del , LRG_121:g.31592_31599del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1257+61_*1257+68del	ENSP00000514307.1:n.*1257+61_*1257+68del
ENST00000525976.6:c.2908+61_2908+68del	ENSP00000434831.2:n.2908+61_2908+68del
ENST00000527481.3:c.2908+61_2908+68del	ENSP00000466340.2:n.2908+61_2908+68del
ENST00000529370.6:n.4284+61_4284+68del
ENST00000529739.2:n.3383_3390del
ENST00000530829.2:c.*2459+61_*2459+68del	ENSP00000436826.2:n.*2459+61_*2459+68del
ENST00000531836.6:c.2908+61_2908+68del	ENSP00000436175.2:n.2908+61_2908+68del
ENST00000533334.2:c.*950+61_*950+68del	ENSP00000432320.2:n.*950+61_*950+68del
ENST00000534228.2:n.4428_4435del
ENST00000699354.1:n.1010+61_1010+68del
ENST00000699355.1:c.*2074_*2081del	ENSP00000514328.1:n.*2074_*2081del
ENST00000699356.1:n.3383_3390del
ENST00000699357.1:n.4428_4435del
ENST00000699358.1:c.2908+61_2908+68del	ENSP00000514329.1:n.2908+61_2908+68del
ENST00000699359.1:c.114+61_114+68del
ENST00000699360.1:c.2908+61_2908+68del	ENSP00000514331.1:n.2908+61_2908+68del
ENST00000699368.1:c.113-52_113-45del	ENSP00000514335.1:n.113-52_113-45del
ENST00000525621.6:c.2908+61_2908+68del MANE Select	ENSP00000431885.1:n.2908+61_2908+68del
ENST00000264818.10:c.2908+61_2908+68del	ENSP00000264818.6:n.2908+61_2908+68del
ENST00000524462.5:c.2353+61_2353+68del	ENSP00000433203.1:n.2353+61_2353+68del
ENST00000525621.5:c.2908+61_2908+68del	ENSP00000431885.1:n.2908+61_2908+68del
ENST00000527481.2:c.204+61_204+68del
ENST00000529412.1:n.641_648del
ENST00000529739.1:c.-358_-351del	ENSP00000436155.1:n.-358_-351del
ENST00000530560.5:c.337+61_337+68del	ENSP00000465291.1:n.337+61_337+68del
ENST00000592137.1:n.62+61_62+68del
NM_003331.4:c.2908+61_2908+68del , LRG_121t1:c.2908+61_2908+68del	NP_003322.3:n.2908+61_2908+68del
XM_011528245.1:c.2908+61_2908+68del	XP_011526547.1:n.2908+61_2908+68del
XM_011528246.1:c.2611+61_2611+68del	XP_011526548.1:n.2611+61_2611+68del
XM_011528247.1:c.2611+61_2611+68del	XP_011526549.1:n.2611+61_2611+68del
XM_011528248.1:c.2908+61_2908+68del	XP_011526550.1:n.2908+61_2908+68del
XM_011528249.1:c.1582+61_1582+68del	XP_011526551.1:n.1582+61_1582+68del
XM_011528251.1:c.1165+61_1165+68del	XP_011526553.1:n.1165+61_1165+68del
XM_011528246.3:c.2611+61_2611+68del	XP_011526548.1:n.2611+61_2611+68del
XM_011528249.2:c.1582+61_1582+68del	XP_011526551.1:n.1582+61_1582+68del
XR_001753750.1:n.3065+61_3065+68del
XR_001753751.1:n.3126_3133del
XR_002958353.1:n.4052_4059del
NM_003331.5:c.2908+61_2908+68del MANE Select	NP_003322.3:n.2908+61_2908+68del
NM_001385197.1:c.2908+61_2908+68del	NP_001372126.1:n.2908+61_2908+68del
NM_001385198.1:c.2908+61_2908+68del	NP_001372127.1:n.2908+61_2908+68del
NM_001385199.1:c.2722+61_2722+68del	NP_001372128.1:n.2722+61_2722+68del
NM_001385200.1:c.2905+61_2905+68del	NP_001372129.1:n.2905+61_2905+68del
NM_001385201.1:c.2710+61_2710+68del	NP_001372130.1:n.2710+61_2710+68del
NM_001385202.1:c.2824+61_2824+68del	NP_001372131.1:n.2824+61_2824+68del
NM_001385203.1:c.2989+61_2989+68del	NP_001372132.1:n.2989+61_2989+68del
NM_001385204.1:c.3118+61_3118+68del	NP_001372133.1:n.3118+61_3118+68del
NM_001385205.1:c.2818+61_2818+68del	NP_001372134.1:n.2818+61_2818+68del
NM_001385206.1:c.2782+61_2782+68del	NP_001372135.1:n.2782+61_2782+68del
NM_001385207.1:c.2890+61_2890+68del	NP_001372136.1:n.2890+61_2890+68del