Canonical Allele Identifier: CA403996126

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10468592G>C (hg19) ; chr19:g.10357916G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10357916G>C , CM000681.2:g.10357916G>C	GRCh38
NC_000019.9:g.10468592G>C , CM000681.1:g.10468592G>C	GRCh37
NC_000019.8:g.10329592G>C	NCBI36
NG_007872.1:g.27657C>G , LRG_121:g.27657C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000524470.2:c.*663C>G	ENSP00000514307.1:n.*663C>G
ENST00000525976.6:c.2314C>G	ENSP00000434831.2:p.Arg772Gly
ENST00000527481.3:c.2314C>G	ENSP00000466340.2:p.Arg772Gly
ENST00000529370.6:n.2645C>G
ENST00000529739.2:n.2728C>G
ENST00000530829.2:c.*1865C>G	ENSP00000436826.2:n.*1865C>G
ENST00000531836.6:c.2314C>G	ENSP00000436175.2:p.Arg772Gly
ENST00000533334.2:c.*356C>G	ENSP00000432320.2:n.*356C>G
ENST00000534228.2:n.2728C>G
ENST00000699354.1:n.416C>G
ENST00000699355.1:c.*374C>G	ENSP00000514328.1:n.*374C>G
ENST00000699356.1:n.2728C>G
ENST00000699357.1:n.2728C>G
ENST00000699358.1:c.2314C>G	ENSP00000514329.1:p.Arg772Gly
ENST00000699360.1:c.2314C>G	ENSP00000514331.1:p.Arg772Gly
ENST00000525621.6:c.2314C>G MANE Select	ENSP00000431885.1:p.Arg772Gly
ENST00000264818.10:c.2314C>G	ENSP00000264818.6:p.Arg772Gly
ENST00000524462.5:c.1759C>G	ENSP00000433203.1:p.Arg587Gly
ENST00000525621.5:c.2314C>G	ENSP00000431885.1:p.Arg772Gly
ENST00000529370.5:c.2314C>G	ENSP00000432728.1:p.Arg772Gly
ENST00000533334.1:c.603C>G
NM_003331.4:c.2314C>G , LRG_121t1:c.2314C>G	NP_003322.3:p.Arg772Gly
XM_011528245.1:c.2314C>G	XP_011526547.1:p.Arg772Gly
XM_011528246.1:c.2017C>G	XP_011526548.1:p.Arg673Gly
XM_011528247.1:c.2017C>G	XP_011526549.1:p.Arg673Gly
XM_011528248.1:c.2314C>G	XP_011526550.1:p.Arg772Gly
XM_011528249.1:c.988C>G	XP_011526551.1:p.Arg330Gly
XM_011528251.1:c.571C>G	XP_011526553.1:p.Arg191Gly
XM_011528246.3:c.2017C>G	XP_011526548.1:p.Arg673Gly
XM_011528249.2:c.988C>G	XP_011526551.1:p.Arg330Gly
XR_001753750.1:n.2471C>G
XR_001753751.1:n.2471C>G
XR_001753752.1:n.2583C>G
XR_002958353.1:n.2352C>G
NM_003331.5:c.2314C>G MANE Select	NP_003322.3:p.Arg772Gly
NM_001385197.1:c.2314C>G	NP_001372126.1:p.Arg772Gly
NM_001385198.1:c.2314C>G	NP_001372127.1:p.Arg772Gly
NM_001385199.1:c.2128C>G	NP_001372128.1:p.Arg710Gly
NM_001385200.1:c.2314C>G	NP_001372129.1:p.Arg772Gly
NM_001385201.1:c.2116C>G	NP_001372130.1:p.Arg706Gly
NM_001385202.1:c.2230C>G	NP_001372131.1:p.Arg744Gly
NM_001385203.1:c.2314C>G	NP_001372132.1:p.Arg772Gly
NM_001385204.1:c.2314C>G	NP_001372133.1:p.Arg772Gly
NM_001385205.1:c.2224C>G	NP_001372134.1:p.Arg742Gly
NM_001385206.1:c.2188C>G	NP_001372135.1:p.Arg730Gly
NM_001385207.1:c.2296C>G	NP_001372136.1:p.Arg766Gly