Canonical Allele Identifier: CA500059836

Gene: STAT5B

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42218267A>T , CM000679.2:g.42218267A>T	GRCh38
NC_000017.10:g.40370285A>T , CM000679.1:g.40370285A>T	GRCh37
NC_000017.9:g.37623811A>T	NCBI36
NG_007271.1:g.63140T>A , LRG_192:g.63140T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415845.2:c.1053T>A	ENSP00000398379.2:p.Thr351=
ENST00000698774.1:n.1227T>A
ENST00000698775.1:c.*1059T>A	ENSP00000513922.1:n.*1059T>A
ENST00000698776.1:c.1053T>A	ENSP00000513923.1:p.Thr351=
ENST00000698777.1:c.1053T>A	ENSP00000513924.1:p.Thr351=
ENST00000698778.1:c.1053T>A	ENSP00000513925.1:p.Thr351=
ENST00000698779.1:c.1053T>A	ENSP00000513926.1:p.Thr351=
ENST00000698801.1:n.929T>A
ENST00000698802.1:c.740T>A	ENSP00000513944.1:n.740T>A
ENST00000698803.1:c.*803T>A	ENSP00000513945.1:n.*803T>A
ENST00000698804.1:n.2786T>A
ENST00000698805.1:n.2396T>A
ENST00000698806.1:c.*767T>A	ENSP00000513946.1:n.*767T>A
ENST00000698807.1:n.2429T>A
ENST00000698808.1:c.1050T>A	ENSP00000513947.1:p.Thr350=
ENST00000698809.1:c.1053T>A	ENSP00000513948.1:p.Thr351=
ENST00000698810.1:c.*803T>A	ENSP00000513949.1:n.*803T>A
ENST00000698812.1:c.*1059T>A	ENSP00000513950.1:n.*1059T>A
ENST00000698813.1:c.1053T>A	ENSP00000513951.1:p.Thr351=
ENST00000698814.1:c.1053T>A	ENSP00000513952.1:p.Thr351=
ENST00000698815.1:c.1053T>A	ENSP00000513953.1:p.Thr351=
ENST00000698816.1:n.1141T>A
ENST00000293328.8:c.1053T>A MANE Select	ENSP00000293328.3:p.Thr351=
ENST00000293328.7:c.1053T>A	ENSP00000293328.3:p.Thr351=
ENST00000468312.1:n.1222T>A
NM_012448.3:c.1053T>A , LRG_192t1:c.1053T>A	NP_036580.2:p.Thr351=
XM_005257625.2:c.771T>A	XP_005257682.1:p.Thr257=
XM_005257626.3:c.1053T>A	XP_005257683.1:p.Thr351=
XM_005257626.4:c.1053T>A	XP_005257683.1:p.Thr351=
XM_017024977.1:c.771T>A	XP_016880466.1:p.Thr257=
XM_024450897.1:c.1053T>A	XP_024306665.1:p.Thr351=
XM_024450898.1:c.1053T>A	XP_024306666.1:p.Thr351=
NM_012448.4:c.1053T>A MANE Select	NP_036580.2:p.Thr351=