Canonical Allele Identifier: CA403988893

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464864T>G (hg19) ; chr19:g.10354188T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354188T>G , CM000681.2:g.10354188T>G	GRCh38
NC_000019.9:g.10464864T>G , CM000681.1:g.10464864T>G	GRCh37
NC_000019.8:g.10325864T>G	NCBI36
NG_007872.1:g.31385A>C , LRG_121:g.31385A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1111A>C	ENSP00000514307.1:n.*1111A>C
ENST00000525976.6:c.2762A>C	ENSP00000434831.2:p.Asp921Ala
ENST00000527481.3:c.2762A>C	ENSP00000466340.2:p.Asp921Ala
ENST00000529370.6:n.4138A>C
ENST00000529739.2:n.3176A>C
ENST00000530829.2:c.*2313A>C	ENSP00000436826.2:n.*2313A>C
ENST00000531836.6:c.2762A>C	ENSP00000436175.2:p.Asp921Ala
ENST00000533334.2:c.*804A>C	ENSP00000432320.2:n.*804A>C
ENST00000534228.2:n.4221A>C
ENST00000699354.1:n.864A>C
ENST00000699355.1:c.*1867A>C	ENSP00000514328.1:n.*1867A>C
ENST00000699356.1:n.3176A>C
ENST00000699357.1:n.4221A>C
ENST00000699358.1:c.2762A>C	ENSP00000514329.1:p.Asp921Ala
ENST00000699360.1:c.2762A>C	ENSP00000514331.1:p.Asp921Ala
ENST00000525621.6:c.2762A>C MANE Select	ENSP00000431885.1:p.Asp921Ala
ENST00000264818.10:c.2762A>C	ENSP00000264818.6:p.Asp921Ala
ENST00000524462.5:c.2207A>C	ENSP00000433203.1:p.Asp736Ala
ENST00000525621.5:c.2762A>C	ENSP00000431885.1:p.Asp921Ala
ENST00000527481.2:c.58A>C
ENST00000529412.1:n.434A>C
ENST00000530560.5:c.191A>C	ENSP00000465291.1:p.Asp64Ala
NM_003331.4:c.2762A>C , LRG_121t1:c.2762A>C	NP_003322.3:p.Asp921Ala
XM_011528245.1:c.2762A>C	XP_011526547.1:p.Asp921Ala
XM_011528246.1:c.2465A>C	XP_011526548.1:p.Asp822Ala
XM_011528247.1:c.2465A>C	XP_011526549.1:p.Asp822Ala
XM_011528248.1:c.2762A>C	XP_011526550.1:p.Asp921Ala
XM_011528249.1:c.1436A>C	XP_011526551.1:p.Asp479Ala
XM_011528251.1:c.1019A>C	XP_011526553.1:p.Asp340Ala
XM_011528246.3:c.2465A>C	XP_011526548.1:p.Asp822Ala
XM_011528249.2:c.1436A>C	XP_011526551.1:p.Asp479Ala
XR_001753750.1:n.2919A>C
XR_001753751.1:n.2919A>C
XR_002958353.1:n.3845A>C
NM_003331.5:c.2762A>C MANE Select	NP_003322.3:p.Asp921Ala
NM_001385197.1:c.2762A>C	NP_001372126.1:p.Asp921Ala
NM_001385198.1:c.2762A>C	NP_001372127.1:p.Asp921Ala
NM_001385199.1:c.2576A>C	NP_001372128.1:p.Asp859Ala
NM_001385200.1:c.2759A>C	NP_001372129.1:p.Asp920Ala
NM_001385201.1:c.2564A>C	NP_001372130.1:p.Asp855Ala
NM_001385202.1:c.2678A>C	NP_001372131.1:p.Asp893Ala
NM_001385203.1:c.2843A>C	NP_001372132.1:p.Asp948Ala
NM_001385204.1:c.2972A>C	NP_001372133.1:p.Asp991Ala
NM_001385205.1:c.2672A>C	NP_001372134.1:p.Asp891Ala
NM_001385206.1:c.2636A>C	NP_001372135.1:p.Asp879Ala
NM_001385207.1:c.2744A>C	NP_001372136.1:p.Asp915Ala