Canonical Allele Identifier: CA631997782

Gene: TYK2

Linked Data

• dbSNP Id: rs1212475961
• gnomAD v2: 19-10464648-GCCCACAAGGCCACA-G
• gnomAD v3: 19-10353972-GCCCACAAGGCCACA-G
• gnomAD v4: 19-10353972-GCCCACAAGGCCACA-G
• MyVariant Identifiers: chr19:g.10464649_10464662del (hg19) ; chr19:g.10353973_10353986del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10353978_10353991del , CM000681.2:g.10353978_10353991del	GRCh38
NC_000019.9:g.10464654_10464667del , CM000681.1:g.10464654_10464667del	GRCh37
NC_000019.8:g.10325654_10325667del	NCBI36
NG_007872.1:g.31587_31600del , LRG_121:g.31587_31600del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1257+56_*1257+69del	ENSP00000514307.1:n.*1257+56_*1257+69del
ENST00000525976.6:c.2908+56_2908+69del	ENSP00000434831.2:n.2908+56_2908+69del
ENST00000527481.3:c.2908+56_2908+69del	ENSP00000466340.2:n.2908+56_2908+69del
ENST00000529370.6:n.4284+56_4284+69del
ENST00000529739.2:n.3378_3391del
ENST00000530829.2:c.*2459+56_*2459+69del	ENSP00000436826.2:n.*2459+56_*2459+69del
ENST00000531836.6:c.2908+56_2908+69del	ENSP00000436175.2:n.2908+56_2908+69del
ENST00000533334.2:c.*950+56_*950+69del	ENSP00000432320.2:n.*950+56_*950+69del
ENST00000534228.2:n.4423_4436del
ENST00000699354.1:n.1010+56_1010+69del
ENST00000699355.1:c.*2069_*2082del	ENSP00000514328.1:n.*2069_*2082del
ENST00000699356.1:n.3378_3391del
ENST00000699357.1:n.4423_4436del
ENST00000699358.1:c.2908+56_2908+69del	ENSP00000514329.1:n.2908+56_2908+69del
ENST00000699359.1:c.114+56_114+69del
ENST00000699360.1:c.2908+56_2908+69del	ENSP00000514331.1:n.2908+56_2908+69del
ENST00000699368.1:c.113-57_113-44del	ENSP00000514335.1:n.113-57_113-44del
ENST00000525621.6:c.2908+56_2908+69del MANE Select	ENSP00000431885.1:n.2908+56_2908+69del
ENST00000264818.10:c.2908+56_2908+69del	ENSP00000264818.6:n.2908+56_2908+69del
ENST00000524462.5:c.2353+56_2353+69del	ENSP00000433203.1:n.2353+56_2353+69del
ENST00000525621.5:c.2908+56_2908+69del	ENSP00000431885.1:n.2908+56_2908+69del
ENST00000527481.2:c.204+56_204+69del
ENST00000529412.1:n.636_649del
ENST00000529739.1:c.-363_-350del	ENSP00000436155.1:n.-363_-350del
ENST00000530560.5:c.337+56_337+69del	ENSP00000465291.1:n.337+56_337+69del
ENST00000592137.1:n.62+56_62+69del
NM_003331.4:c.2908+56_2908+69del , LRG_121t1:c.2908+56_2908+69del	NP_003322.3:n.2908+56_2908+69del
XM_011528245.1:c.2908+56_2908+69del	XP_011526547.1:n.2908+56_2908+69del
XM_011528246.1:c.2611+56_2611+69del	XP_011526548.1:n.2611+56_2611+69del
XM_011528247.1:c.2611+56_2611+69del	XP_011526549.1:n.2611+56_2611+69del
XM_011528248.1:c.2908+56_2908+69del	XP_011526550.1:n.2908+56_2908+69del
XM_011528249.1:c.1582+56_1582+69del	XP_011526551.1:n.1582+56_1582+69del
XM_011528251.1:c.1165+56_1165+69del	XP_011526553.1:n.1165+56_1165+69del
XM_011528246.3:c.2611+56_2611+69del	XP_011526548.1:n.2611+56_2611+69del
XM_011528249.2:c.1582+56_1582+69del	XP_011526551.1:n.1582+56_1582+69del
XR_001753750.1:n.3065+56_3065+69del
XR_001753751.1:n.3121_3134del
XR_002958353.1:n.4047_4060del
NM_003331.5:c.2908+56_2908+69del MANE Select	NP_003322.3:n.2908+56_2908+69del
NM_001385197.1:c.2908+56_2908+69del	NP_001372126.1:n.2908+56_2908+69del
NM_001385198.1:c.2908+56_2908+69del	NP_001372127.1:n.2908+56_2908+69del
NM_001385199.1:c.2722+56_2722+69del	NP_001372128.1:n.2722+56_2722+69del
NM_001385200.1:c.2905+56_2905+69del	NP_001372129.1:n.2905+56_2905+69del
NM_001385201.1:c.2710+56_2710+69del	NP_001372130.1:n.2710+56_2710+69del
NM_001385202.1:c.2824+56_2824+69del	NP_001372131.1:n.2824+56_2824+69del
NM_001385203.1:c.2989+56_2989+69del	NP_001372132.1:n.2989+56_2989+69del
NM_001385204.1:c.3118+56_3118+69del	NP_001372133.1:n.3118+56_3118+69del
NM_001385205.1:c.2818+56_2818+69del	NP_001372134.1:n.2818+56_2818+69del
NM_001385206.1:c.2782+56_2782+69del	NP_001372135.1:n.2782+56_2782+69del
NM_001385207.1:c.2890+56_2890+69del	NP_001372136.1:n.2890+56_2890+69del