Canonical Allele Identifier: CA2322386883

Gene: TYK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352076_10352081delinsCGTCCT , CM000681.2:g.10352076_10352081delinsCGTCCT	GRCh38
NC_000019.9:g.10462752_10462757delinsCGTCCT , CM000681.1:g.10462752_10462757delinsCGTCCT	GRCh37
NC_000019.8:g.10323752_10323757delinsCGTCCT	NCBI36
NG_007872.1:g.33492_33497delinsAGGACG , LRG_121:g.33492_33497delinsAGGACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1667+353_*1667+358delinsAGGACG	ENSP00000514307.1:n.*1667+353_*1667+358delinsAGGACG
ENST00000525976.6:c.3318+353_3318+358delinsAGGACG	ENSP00000434831.2:n.3318+353_3318+358delinsAGGACG
ENST00000527481.3:c.*88+353_*88+358delinsAGGACG	ENSP00000466340.2:n.*88+353_*88+358delinsAGGACG
ENST00000529370.6:n.4694+353_4694+358delinsAGGACG
ENST00000529739.2:n.4127+353_4127+358delinsAGGACG
ENST00000530829.2:c.*2869+353_*2869+358delinsAGGACG	ENSP00000436826.2:n.*2869+353_*2869+358delinsAGGACG
ENST00000531836.6:c.3318+353_3318+358delinsAGGACG	ENSP00000436175.2:n.3318+353_3318+358delinsAGGACG
ENST00000533334.2:c.*1242+845_*1242+850delinsAGGACG	ENSP00000432320.2:n.*1242+845_*1242+850delinsAGGACG
ENST00000534228.2:n.5054+845_5054+850delinsAGGACG
ENST00000699354.1:n.1420+353_1420+358delinsAGGACG
ENST00000699355.1:c.*2818+353_*2818+358delinsAGGACG	ENSP00000514328.1:n.*2818+353_*2818+358delinsAGGACG
ENST00000699356.1:n.4127+353_4127+358delinsAGGACG
ENST00000699357.1:n.5172+353_5172+358delinsAGGACG
ENST00000699358.1:c.3200+845_3200+850delinsAGGACG	ENSP00000514329.1:n.3200+845_3200+850delinsAGGACG
ENST00000699359.1:c.492+353_492+358delinsAGGACG
ENST00000699360.1:c.3276+353_3276+358delinsAGGACG	ENSP00000514331.1:n.3276+353_3276+358delinsAGGACG
ENST00000699361.1:n.352+353_352+358delinsAGGACG
ENST00000699362.1:c.214+353_214+358delinsAGGACG	ENSP00000514332.1:n.214+353_214+358delinsAGGACG
ENST00000699363.1:c.214+353_214+358delinsAGGACG	ENSP00000514333.1:n.214+353_214+358delinsAGGACG
ENST00000699364.1:n.318+353_318+358delinsAGGACG
ENST00000699365.1:c.387+353_387+358delinsAGGACG	ENSP00000514334.1:n.387+353_387+358delinsAGGACG
ENST00000699366.1:n.112-1113_112-1108delinsAGGACG
ENST00000699367.1:n.112-919_112-914delinsAGGACG
ENST00000699368.1:c.805+353_805+358delinsAGGACG	ENSP00000514335.1:n.805+353_805+358delinsAGGACG
ENST00000525621.6:c.3318+353_3318+358delinsAGGACG MANE Select	ENSP00000431885.1:n.3318+353_3318+358delinsAGGACG
ENST00000264818.10:c.3318+353_3318+358delinsAGGACG	ENSP00000264818.6:n.3318+353_3318+358delinsAGGACG
ENST00000524462.5:c.2763+353_2763+358delinsAGGACG	ENSP00000433203.1:n.2763+353_2763+358delinsAGGACG
ENST00000525621.5:c.3318+353_3318+358delinsAGGACG	ENSP00000431885.1:n.3318+353_3318+358delinsAGGACG
ENST00000525976.5:c.59+353_59+358delinsAGGACG
ENST00000527481.2:c.495+353_495+358delinsAGGACG
ENST00000529422.1:n.117-788_117-783delinsAGGACG
ENST00000530220.1:n.331+845_331+850delinsAGGACG
ENST00000530560.5:c.338-1113_338-1108delinsAGGACG	ENSP00000465291.1:n.338-1113_338-1108delinsAGGACG
ENST00000592137.1:n.472+353_472+358delinsAGGACG
NM_003331.4:c.3318+353_3318+358delinsAGGACG , LRG_121t1:c.3318+353_3318+358delinsAGGACG	NP_003322.3:n.3318+353_3318+358delinsAGGACG
XM_011528245.1:c.3318+353_3318+358delinsAGGACG	XP_011526547.1:n.3318+353_3318+358delinsAGGACG
XM_011528246.1:c.3021+353_3021+358delinsAGGACG	XP_011526548.1:n.3021+353_3021+358delinsAGGACG
XM_011528247.1:c.3021+353_3021+358delinsAGGACG	XP_011526549.1:n.3021+353_3021+358delinsAGGACG
XM_011528248.1:c.3200+845_3200+850delinsAGGACG	XP_011526550.1:n.3200+845_3200+850delinsAGGACG
XM_011528249.1:c.1992+353_1992+358delinsAGGACG	XP_011526551.1:n.1992+353_1992+358delinsAGGACG
XM_011528251.1:c.1575+353_1575+358delinsAGGACG	XP_011526553.1:n.1575+353_1575+358delinsAGGACG
XM_011528246.3:c.3021+353_3021+358delinsAGGACG	XP_011526548.1:n.3021+353_3021+358delinsAGGACG
XM_011528249.2:c.1992+353_1992+358delinsAGGACG	XP_011526551.1:n.1992+353_1992+358delinsAGGACG
XR_001753750.1:n.3357+845_3357+850delinsAGGACG
XR_001753751.1:n.3870+353_3870+358delinsAGGACG
XR_002958353.1:n.4796+353_4796+358delinsAGGACG
NM_003331.5:c.3318+353_3318+358delinsAGGACG MANE Select	NP_003322.3:n.3318+353_3318+358delinsAGGACG
NM_001385197.1:c.3318+353_3318+358delinsAGGACG	NP_001372126.1:n.3318+353_3318+358delinsAGGACG
NM_001385198.1:c.3168+877_3168+882delinsAGGACG	NP_001372127.1:n.3168+877_3168+882delinsAGGACG
NM_001385199.1:c.3132+353_3132+358delinsAGGACG	NP_001372128.1:n.3132+353_3132+358delinsAGGACG
NM_001385200.1:c.3315+353_3315+358delinsAGGACG	NP_001372129.1:n.3315+353_3315+358delinsAGGACG
NM_001385201.1:c.3120+353_3120+358delinsAGGACG	NP_001372130.1:n.3120+353_3120+358delinsAGGACG
NM_001385202.1:c.3234+353_3234+358delinsAGGACG	NP_001372131.1:n.3234+353_3234+358delinsAGGACG
NM_001385203.1:c.3399+353_3399+358delinsAGGACG	NP_001372132.1:n.3399+353_3399+358delinsAGGACG
NM_001385204.1:c.3528+353_3528+358delinsAGGACG	NP_001372133.1:n.3528+353_3528+358delinsAGGACG
NM_001385205.1:c.3228+353_3228+358delinsAGGACG	NP_001372134.1:n.3228+353_3228+358delinsAGGACG
NM_001385206.1:c.3192+353_3192+358delinsAGGACG	NP_001372135.1:n.3192+353_3192+358delinsAGGACG
NM_001385207.1:c.3300+353_3300+358delinsAGGACG	NP_001372136.1:n.3300+353_3300+358delinsAGGACG