Canonical Allele Identifier: CA658658160
Gene: STAT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 475691
ClinVar RCV Id: RCV000537740
dbSNP Id: rs1555169006

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56343472_56343473delinsAG , CM000674.2:g.56343472_56343473delinsAG GRCh38
NC_000012.11:g.56737256_56737257delinsAG , CM000674.1:g.56737256_56737257delinsAG GRCh37
NC_000012.10:g.55023523_55023524delinsAG NCBI36
NG_046314.1:g.21781_21782delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000555488.2:n.2355_2356delinsCT
ENST00000698178.1:n.3063_3064delinsCT
ENST00000698179.1:n.3015_3016delinsCT
ENST00000698180.1:c.*2227_*2228delinsCT ENSP00000513597.1:n.*2227_*2228delinsCT
ENST00000698181.1:n.3509_3510delinsCT
ENST00000698182.1:n.3282_3283delinsCT
ENST00000698183.1:n.3742_3743delinsCT
ENST00000698184.1:n.3516_3517delinsCT
ENST00000698185.1:n.3675_3676delinsCT
ENST00000698186.1:c.2340_2341delinsCT ENSP00000513598.1:p.Gly781Cys
ENST00000698187.1:n.2787_2788delinsCT
ENST00000698188.1:n.3139_3140delinsCT
ENST00000698189.1:n.4549_4550delinsCT
ENST00000698190.1:n.3130_3131delinsCT
ENST00000698191.1:n.3063_3064delinsCT
ENST00000698192.1:c.2472_2473delinsCT ENSP00000513599.1:p.Gly825Cys
ENST00000698193.1:c.*344_*345delinsCT ENSP00000513600.1:n.*344_*345delinsCT
ENST00000314128.9:c.2472_2473delinsCT MANE Select ENSP00000315768.4:p.Gly825Cys
ENST00000556140.6:n.3244_3245delinsCT
ENST00000650805.1:c.*1906_*1907delinsCT ENSP00000498710.1:n.*1906_*1907delinsCT
ENST00000651078.1:n.3125_3126delinsCT
ENST00000651301.1:c.*2146_*2147delinsCT ENSP00000498470.1:n.*2146_*2147delinsCT
ENST00000651339.1:n.1207_1208delinsCT
ENST00000651805.1:n.2861_2862delinsCT
ENST00000651915.1:c.2373_2374delinsCT ENSP00000498876.1:p.Gly792Cys
ENST00000651934.1:n.2912_2913delinsCT
ENST00000651967.1:n.2587_2588delinsCT
ENST00000652091.1:n.2990_2991delinsCT
ENST00000652398.1:c.*2038_*2039delinsCT ENSP00000499022.1:n.*2038_*2039delinsCT
ENST00000652624.1:c.*1598_*1599delinsCT ENSP00000499108.1:n.*1598_*1599delinsCT
ENST00000652741.1:c.*2227_*2228delinsCT ENSP00000498704.1:n.*2227_*2228delinsCT
ENST00000314128.8:c.2472_2473delinsCT ENSP00000315768.4:p.Gly825Cys
ENST00000556539.5:n.1402_1403delinsCT
ENST00000557235.5:c.2460_2461delinsCT ENSP00000450751.1:p.Gly821Cys
NM_005419.3:c.2472_2473delinsCT NP_005410.1:p.Gly825Cys
NM_198332.1:c.2460_2461delinsCT NP_938146.1:p.Gly821Cys
XM_011538697.1:c.2496_2497delinsCT XP_011536999.1:p.Gly833Cys
XM_011538698.1:c.2484_2485delinsCT XP_011537000.1:p.Gly829Cys
XM_011538700.1:c.1764_1765delinsCT XP_011537002.1:p.Gly589Cys
XM_011538701.1:c.1527_1528delinsCT XP_011537003.1:p.Gly510Cys
XM_011538697.2:c.2496_2497delinsCT XP_011536999.1:p.Gly833Cys
XM_011538698.3:c.2484_2485delinsCT XP_011537000.1:p.Gly829Cys
XM_011538700.2:c.1764_1765delinsCT XP_011537002.1:p.Gly589Cys
XM_017019904.2:c.1740_1741delinsCT XP_016875393.1:p.Gly581Cys
XR_001748856.1:n.2395_2396delinsCT
XR_001748857.1:n.2476_2477delinsCT
XR_001748858.2:n.2353_2354delinsCT
XR_002957375.1:n.2767_2768delinsCT
XR_002957376.1:n.2725_2726delinsCT
NM_005419.4:c.2472_2473delinsCT MANE Select NP_005410.1:p.Gly825Cys
NM_198332.2:c.2460_2461delinsCT NP_938146.1:p.Gly821Cys
NM_001385110.1:c.2439_2440delinsCT NP_001372039.1:p.Gly814Cys
NM_001385111.1:c.2373_2374delinsCT NP_001372040.1:p.Gly792Cys
NM_001385113.1:c.*41_*42delinsCT NP_001372042.1:n.*41_*42delinsCT
NM_001385114.1:c.2451_2452delinsCT NP_001372043.1:p.Gly818Cys
NM_001385115.1:c.2430_2431delinsCT NP_001372044.1:p.Gly811Cys