Canonical Allele Identifier: CA305198081

Gene: TYK2

Linked Data

• dbSNP Id: rs958274716
• gnomAD v3: 19-10358036-G-C
• gnomAD v4: 19-10358036-G-C
• MyVariant Identifiers: chr19:g.10468712G>C (hg19) ; chr19:g.10358036G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10358036G>C , CM000681.2:g.10358036G>C	GRCh38
NC_000019.9:g.10468712G>C , CM000681.1:g.10468712G>C	GRCh37
NC_000019.8:g.10329712G>C	NCBI36
NG_007872.1:g.27537C>G , LRG_121:g.27537C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*627C>G	ENSP00000514307.1:n.*627C>G
ENST00000525976.6:c.2278C>G	ENSP00000434831.2:p.Pro760Ala
ENST00000527481.3:c.2278C>G	ENSP00000466340.2:p.Pro760Ala
ENST00000529370.6:n.2609C>G
ENST00000529739.2:n.2692C>G
ENST00000530829.2:c.*1829C>G	ENSP00000436826.2:n.*1829C>G
ENST00000531836.6:c.2278C>G	ENSP00000436175.2:p.Pro760Ala
ENST00000533334.2:c.*320C>G	ENSP00000432320.2:n.*320C>G
ENST00000534228.2:n.2692C>G
ENST00000699354.1:n.380C>G
ENST00000699355.1:c.*338C>G	ENSP00000514328.1:n.*338C>G
ENST00000699356.1:n.2692C>G
ENST00000699357.1:n.2692C>G
ENST00000699358.1:c.2278C>G	ENSP00000514329.1:p.Pro760Ala
ENST00000699360.1:c.2278C>G	ENSP00000514331.1:p.Pro760Ala
ENST00000525621.6:c.2278C>G MANE Select	ENSP00000431885.1:p.Pro760Ala
ENST00000264818.10:c.2278C>G	ENSP00000264818.6:p.Pro760Ala
ENST00000524462.5:c.1723C>G	ENSP00000433203.1:p.Pro575Ala
ENST00000525621.5:c.2278C>G	ENSP00000431885.1:p.Pro760Ala
ENST00000529370.5:c.2278C>G	ENSP00000432728.1:p.Pro760Ala
ENST00000533334.1:c.567C>G
NM_003331.4:c.2278C>G , LRG_121t1:c.2278C>G	NP_003322.3:p.Pro760Ala
XM_011528245.1:c.2278C>G	XP_011526547.1:p.Pro760Ala
XM_011528246.1:c.1981C>G	XP_011526548.1:p.Pro661Ala
XM_011528247.1:c.1981C>G	XP_011526549.1:p.Pro661Ala
XM_011528248.1:c.2278C>G	XP_011526550.1:p.Pro760Ala
XM_011528249.1:c.952C>G	XP_011526551.1:p.Pro318Ala
XM_011528251.1:c.535C>G	XP_011526553.1:p.Pro179Ala
XM_011528246.3:c.1981C>G	XP_011526548.1:p.Pro661Ala
XM_011528249.2:c.952C>G	XP_011526551.1:p.Pro318Ala
XR_001753750.1:n.2435C>G
XR_001753751.1:n.2435C>G
XR_001753752.1:n.2547C>G
XR_002958353.1:n.2316C>G
NM_003331.5:c.2278C>G MANE Select	NP_003322.3:p.Pro760Ala
NM_001385197.1:c.2278C>G	NP_001372126.1:p.Pro760Ala
NM_001385198.1:c.2278C>G	NP_001372127.1:p.Pro760Ala
NM_001385199.1:c.2092C>G	NP_001372128.1:p.Pro698Ala
NM_001385200.1:c.2278C>G	NP_001372129.1:p.Pro760Ala
NM_001385201.1:c.2080C>G	NP_001372130.1:p.Pro694Ala
NM_001385202.1:c.2194C>G	NP_001372131.1:p.Pro732Ala
NM_001385203.1:c.2278C>G	NP_001372132.1:p.Pro760Ala
NM_001385204.1:c.2278C>G	NP_001372133.1:p.Pro760Ala
NM_001385205.1:c.2188C>G	NP_001372134.1:p.Pro730Ala
NM_001385206.1:c.2152C>G	NP_001372135.1:p.Pro718Ala
NM_001385207.1:c.2260C>G	NP_001372136.1:p.Pro754Ala