Canonical Allele Identifier: CA11134308
Gene: STAT1 HGNC NCBI

Linked Data

dbSNP Id: rs2280232

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.190986040C>A , CM000664.2:g.190986040C>A GRCh38
NC_000002.11:g.191850766C>A , CM000664.1:g.191850766C>A GRCh37
NC_000002.10:g.191559011C>A NCBI36
NG_008294.1:g.33211G>T , LRG_111:g.33211G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000698141.1:c.1222-380G>T ENSP00000513582.1:n.1222-380G>T
ENST00000698142.1:c.1162-380G>T ENSP00000513583.1:n.1162-380G>T
ENST00000698143.1:n.1382-380G>T
ENST00000698144.1:c.*548-380G>T ENSP00000513584.1:n.*548-380G>T
ENST00000698145.1:c.633+12177G>T ENSP00000513585.1:n.633+12177G>T
ENST00000698146.1:c.*972-380G>T ENSP00000513586.1:n.*972-380G>T
ENST00000698147.1:n.2362G>T
ENST00000698148.1:n.1549-380G>T
ENST00000698149.1:c.1222-380G>T ENSP00000513587.1:n.1222-380G>T
ENST00000698151.1:n.1549-380G>T
ENST00000361099.8:c.1222-380G>T MANE Select ENSP00000354394.4:n.1222-380G>T
ENST00000415035.2:c.1222-380G>T ENSP00000388240.2:n.1222-380G>T
ENST00000423282.2:c.129-9015G>T ENSP00000388772.2:n.129-9015G>T
ENST00000452281.6:c.*548-380G>T ENSP00000394512.1:n.*548-380G>T
ENST00000540176.6:c.1222-380G>T ENSP00000438703.2:n.1222-380G>T
ENST00000673734.1:c.*389-380G>T ENSP00000501040.1:n.*389-380G>T
ENST00000673777.1:c.1216-380G>T ENSP00000500982.1:n.1216-380G>T
ENST00000673816.1:c.1222-380G>T ENSP00000501127.1:n.1222-380G>T
ENST00000673841.1:c.1222-380G>T ENSP00000501225.1:n.1222-380G>T
ENST00000673847.1:c.1222-380G>T ENSP00000501185.1:n.1222-380G>T
ENST00000673858.1:c.*548-380G>T ENSP00000501196.1:n.*548-380G>T
ENST00000673859.1:n.1521-380G>T
ENST00000673863.1:c.39-2282G>T ENSP00000501286.1:n.39-2282G>T
ENST00000673885.1:c.1222-380G>T ENSP00000501159.1:n.1222-380G>T
ENST00000673942.1:c.1216-380G>T ENSP00000501145.1:n.1216-380G>T
ENST00000673952.1:c.1222-380G>T ENSP00000501115.1:n.1222-380G>T
ENST00000674028.1:n.311-8999G>T
ENST00000674080.1:c.1222-380G>T ENSP00000501164.1:n.1222-380G>T
ENST00000674081.1:c.1222-380G>T ENSP00000501289.1:n.1222-380G>T
ENST00000674153.1:c.1222-380G>T ENSP00000501120.1:n.1222-380G>T
ENST00000361099.7:c.1222-380G>T ENSP00000354394.3:n.1222-380G>T
ENST00000392322.7:c.1222-380G>T ENSP00000376136.3:n.1222-380G>T
ENST00000392323.6:c.1228-380G>T ENSP00000376137.2:n.1228-380G>T
ENST00000409465.5:c.1222-380G>T ENSP00000386244.1:n.1222-380G>T
ENST00000452281.5:c.*548-380G>T ENSP00000394512.1:n.*548-380G>T
ENST00000540176.5:c.*548-380G>T ENSP00000438703.1:n.*548-380G>T
NM_007315.3:c.1222-380G>T , LRG_111t1:c.1222-380G>T NP_009330.1:n.1222-380G>T
NM_139266.2:c.1222-380G>T NP_644671.1:n.1222-380G>T
XM_006712718.1:c.1222-380G>T XP_006712781.1:n.1222-380G>T
XM_017004783.2:c.1228-380G>T XP_016860272.1:n.1228-380G>T
XR_001738914.2:n.1615-380G>T
XR_001738915.2:n.1557-380G>T
NM_007315.4:c.1222-380G>T MANE Select NP_009330.1:n.1222-380G>T
NM_001384880.1:c.1162-380G>T NP_001371809.1:n.1162-380G>T
NM_001384881.1:c.1228-380G>T NP_001371810.1:n.1228-380G>T
NM_001384882.1:c.1216-380G>T NP_001371811.1:n.1216-380G>T
NM_001384883.1:c.1123-380G>T NP_001371812.1:n.1123-380G>T
NM_001384884.1:c.1228-380G>T NP_001371813.1:n.1228-380G>T
NM_001384885.1:c.1063-380G>T NP_001371814.1:n.1063-380G>T
NM_001384886.1:c.1222-380G>T NP_001371815.1:n.1222-380G>T
NM_001384887.1:c.1129-380G>T NP_001371816.1:n.1129-380G>T
NM_001384888.1:c.1192-380G>T NP_001371817.1:n.1192-380G>T
NM_001384889.1:c.1222-380G>T NP_001371818.1:n.1222-380G>T
NM_001384890.1:c.1132-380G>T NP_001371819.1:n.1132-380G>T
NM_001384891.1:c.1258-380G>T NP_001371820.1:n.1258-380G>T
NM_139266.3:c.1222-380G>T NP_644671.1:n.1222-380G>T