Canonical Allele Identifier: CA2038331027

Gene: STAT2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56344189A>T , CM000674.2:g.56344189A>T	GRCh38
NC_000012.11:g.56737973A>T , CM000674.1:g.56737973A>T	GRCh37
NC_000012.10:g.55024240A>T	NCBI36
NG_046314.1:g.21065T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555488.2:n.1693-54T>A
ENST00000698178.1:n.2694-54T>A
ENST00000698179.1:n.2646-54T>A
ENST00000698180.1:c.*1858-54T>A	ENSP00000513597.1:n.*1858-54T>A
ENST00000698181.1:n.3140-54T>A
ENST00000698182.1:n.2913-54T>A
ENST00000698183.1:n.3373-54T>A
ENST00000698184.1:n.3147-54T>A
ENST00000698185.1:n.3306-54T>A
ENST00000698186.1:c.1971-54T>A	ENSP00000513598.1:n.1971-54T>A
ENST00000698187.1:n.2418-54T>A
ENST00000698188.1:n.2770-54T>A
ENST00000698189.1:n.3887-54T>A
ENST00000698190.1:n.2761-54T>A
ENST00000698191.1:n.2694-54T>A
ENST00000698192.1:c.2103-54T>A	ENSP00000513599.1:n.2103-54T>A
ENST00000698193.1:c.2103-54T>A	ENSP00000513600.1:n.2103-54T>A
ENST00000314128.9:c.2103-54T>A MANE Select	ENSP00000315768.4:n.2103-54T>A
ENST00000556140.6:n.2875-54T>A
ENST00000650805.1:c.*1537-54T>A	ENSP00000498710.1:n.*1537-54T>A
ENST00000651078.1:n.2756-54T>A
ENST00000651301.1:c.*1777-54T>A	ENSP00000498470.1:n.*1777-54T>A
ENST00000651339.1:n.838-54T>A
ENST00000651805.1:n.2492-54T>A
ENST00000651915.1:c.2004-54T>A	ENSP00000498876.1:n.2004-54T>A
ENST00000651934.1:n.2543-54T>A
ENST00000651967.1:n.2218-54T>A
ENST00000652091.1:n.2621-54T>A
ENST00000652398.1:c.*1669-54T>A	ENSP00000499022.1:n.*1669-54T>A
ENST00000652624.1:c.*1229-54T>A	ENSP00000499108.1:n.*1229-54T>A
ENST00000652741.1:c.*1858-54T>A	ENSP00000498704.1:n.*1858-54T>A
ENST00000314128.8:c.2103-54T>A	ENSP00000315768.4:n.2103-54T>A
ENST00000555488.1:n.486-54T>A
ENST00000556539.5:n.1033-54T>A
ENST00000557235.5:c.2091-54T>A	ENSP00000450751.1:n.2091-54T>A
NM_005419.3:c.2103-54T>A	NP_005410.1:n.2103-54T>A
NM_198332.1:c.2091-54T>A	NP_938146.1:n.2091-54T>A
XM_011538697.1:c.2127-54T>A	XP_011536999.1:n.2127-54T>A
XM_011538698.1:c.2115-54T>A	XP_011537000.1:n.2115-54T>A
XM_011538700.1:c.1395-54T>A	XP_011537002.1:n.1395-54T>A
XM_011538701.1:c.1158-54T>A	XP_011537003.1:n.1158-54T>A
XM_011538697.2:c.2127-54T>A	XP_011536999.1:n.2127-54T>A
XM_011538698.3:c.2115-54T>A	XP_011537000.1:n.2115-54T>A
XM_011538700.2:c.1395-54T>A	XP_011537002.1:n.1395-54T>A
XM_017019904.2:c.1371-54T>A	XP_016875393.1:n.1371-54T>A
XR_001748856.1:n.2026-54T>A
XR_001748857.1:n.2107-54T>A
XR_001748858.2:n.1984-54T>A
XR_002957375.1:n.2398-54T>A
XR_002957376.1:n.2356-54T>A
NM_005419.4:c.2103-54T>A MANE Select	NP_005410.1:n.2103-54T>A
NM_198332.2:c.2091-54T>A	NP_938146.1:n.2091-54T>A
NM_001385110.1:c.2070-54T>A	NP_001372039.1:n.2070-54T>A
NM_001385111.1:c.2004-54T>A	NP_001372040.1:n.2004-54T>A
NM_001385113.1:c.2103-54T>A	NP_001372042.1:n.2103-54T>A
NM_001385114.1:c.2082-54T>A	NP_001372043.1:n.2082-54T>A
NM_001385115.1:c.2061-54T>A	NP_001372044.1:n.2061-54T>A