Canonical Allele Identifier: CA2741611711

Gene: TYK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352733T>G , CM000681.2:g.10352733T>G	GRCh38
NC_000019.9:g.10463409T>G , CM000681.1:g.10463409T>G	GRCh37
NC_000019.8:g.10324409T>G	NCBI36
NG_007872.1:g.32840A>C , LRG_121:g.32840A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1550-182A>C	ENSP00000514307.1:n.*1550-182A>C
ENST00000525976.6:c.3201-182A>C	ENSP00000434831.2:n.3201-182A>C
ENST00000527481.3:c.3082-182A>C	ENSP00000466340.2:n.3082-182A>C
ENST00000529370.6:n.4577-182A>C
ENST00000529739.2:n.4010-182A>C
ENST00000530829.2:c.*2752-182A>C	ENSP00000436826.2:n.*2752-182A>C
ENST00000531836.6:c.3201-182A>C	ENSP00000436175.2:n.3201-182A>C
ENST00000533334.2:c.*1242+193A>C	ENSP00000432320.2:n.*1242+193A>C
ENST00000534228.2:n.5054+193A>C
ENST00000699354.1:n.1303-182A>C
ENST00000699355.1:c.*2701-182A>C	ENSP00000514328.1:n.*2701-182A>C
ENST00000699356.1:n.4010-182A>C
ENST00000699357.1:n.5055-182A>C
ENST00000699358.1:c.3200+193A>C	ENSP00000514329.1:n.3200+193A>C
ENST00000699359.1:c.375-182A>C
ENST00000699360.1:c.3159-182A>C	ENSP00000514331.1:n.3159-182A>C
ENST00000699361.1:n.53A>C
ENST00000699362.1:c.97-182A>C	ENSP00000514332.1:n.97-182A>C
ENST00000699363.1:c.97-182A>C	ENSP00000514333.1:n.97-182A>C
ENST00000699364.1:n.201-182A>C
ENST00000699365.1:c.270-182A>C	ENSP00000514334.1:n.270-182A>C
ENST00000699366.1:n.111+1081A>C
ENST00000699367.1:n.111+1081A>C
ENST00000699368.1:c.688-182A>C	ENSP00000514335.1:n.688-182A>C
ENST00000525621.6:c.3201-182A>C MANE Select	ENSP00000431885.1:n.3201-182A>C
ENST00000264818.10:c.3201-182A>C	ENSP00000264818.6:n.3201-182A>C
ENST00000524462.5:c.2646-182A>C	ENSP00000433203.1:n.2646-182A>C
ENST00000525621.5:c.3201-182A>C	ENSP00000431885.1:n.3201-182A>C
ENST00000527481.2:c.378-182A>C
ENST00000529422.1:n.116+289A>C
ENST00000529739.1:c.270-182A>C	ENSP00000436155.1:n.270-182A>C
ENST00000530220.1:n.331+193A>C
ENST00000530560.5:c.337+1309A>C	ENSP00000465291.1:n.337+1309A>C
ENST00000592137.1:n.355-182A>C
NM_003331.4:c.3201-182A>C , LRG_121t1:c.3201-182A>C	NP_003322.3:n.3201-182A>C
XM_011528245.1:c.3201-182A>C	XP_011526547.1:n.3201-182A>C
XM_011528246.1:c.2904-182A>C	XP_011526548.1:n.2904-182A>C
XM_011528247.1:c.2904-182A>C	XP_011526549.1:n.2904-182A>C
XM_011528248.1:c.3200+193A>C	XP_011526550.1:n.3200+193A>C
XM_011528249.1:c.1875-182A>C	XP_011526551.1:n.1875-182A>C
XM_011528251.1:c.1458-182A>C	XP_011526553.1:n.1458-182A>C
XM_011528246.3:c.2904-182A>C	XP_011526548.1:n.2904-182A>C
XM_011528249.2:c.1875-182A>C	XP_011526551.1:n.1875-182A>C
XR_001753750.1:n.3357+193A>C
XR_001753751.1:n.3753-182A>C
XR_002958353.1:n.4679-182A>C
NM_003331.5:c.3201-182A>C MANE Select	NP_003322.3:n.3201-182A>C
NM_001385197.1:c.3201-182A>C	NP_001372126.1:n.3201-182A>C
NM_001385198.1:c.3168+225A>C	NP_001372127.1:n.3168+225A>C
NM_001385199.1:c.3015-182A>C	NP_001372128.1:n.3015-182A>C
NM_001385200.1:c.3198-182A>C	NP_001372129.1:n.3198-182A>C
NM_001385201.1:c.3003-182A>C	NP_001372130.1:n.3003-182A>C
NM_001385202.1:c.3117-182A>C	NP_001372131.1:n.3117-182A>C
NM_001385203.1:c.3282-182A>C	NP_001372132.1:n.3282-182A>C
NM_001385204.1:c.3411-182A>C	NP_001372133.1:n.3411-182A>C
NM_001385205.1:c.3111-182A>C	NP_001372134.1:n.3111-182A>C
NM_001385206.1:c.3075-182A>C	NP_001372135.1:n.3075-182A>C
NM_001385207.1:c.3183-182A>C	NP_001372136.1:n.3183-182A>C