Canonical Allele Identifier: CA2963269630

Gene: STAT5B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42218274_42218275insGC , CM000679.2:g.42218274_42218275insGC	GRCh38
NC_000017.10:g.40370292_40370293insGC , CM000679.1:g.40370292_40370293insGC	GRCh37
NC_000017.9:g.37623818_37623819insGC	NCBI36
NG_007271.1:g.63132_63133insGC , LRG_192:g.63132_63133insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415845.2:c.1045_1046insGC	ENSP00000398379.2:p.Ala349GlyfsTer13
ENST00000698774.1:n.1219_1220insGC
ENST00000698775.1:c.*1051_*1052insGC	ENSP00000513922.1:n.*1051_*1052insGC
ENST00000698776.1:c.1045_1046insGC	ENSP00000513923.1:p.Ala349GlyfsTer13
ENST00000698777.1:c.1045_1046insGC	ENSP00000513924.1:p.Ala349GlyfsTer13
ENST00000698778.1:c.1045_1046insGC	ENSP00000513925.1:p.Ala349GlyfsTer13
ENST00000698779.1:c.1045_1046insGC	ENSP00000513926.1:p.Ala349GlyfsTer13
ENST00000698801.1:n.921_922insGC
ENST00000698802.1:c.732_733insGC	ENSP00000513944.1:n.732_733insGC
ENST00000698803.1:c.*795_*796insGC	ENSP00000513945.1:n.*795_*796insGC
ENST00000698804.1:n.2778_2779insGC
ENST00000698805.1:n.2388_2389insGC
ENST00000698806.1:c.*759_*760insGC	ENSP00000513946.1:n.*759_*760insGC
ENST00000698807.1:n.2421_2422insGC
ENST00000698808.1:c.1042_1043insGC	ENSP00000513947.1:p.Ala348GlyfsTer13
ENST00000698809.1:c.1045_1046insGC	ENSP00000513948.1:p.Ala349GlyfsTer13
ENST00000698810.1:c.*795_*796insGC	ENSP00000513949.1:n.*795_*796insGC
ENST00000698812.1:c.*1051_*1052insGC	ENSP00000513950.1:n.*1051_*1052insGC
ENST00000698813.1:c.1045_1046insGC	ENSP00000513951.1:p.Ala349GlyfsTer13
ENST00000698814.1:c.1045_1046insGC	ENSP00000513952.1:p.Ala349GlyfsTer13
ENST00000698815.1:c.1045_1046insGC	ENSP00000513953.1:p.Ala349GlyfsTer13
ENST00000698816.1:n.1133_1134insGC
ENST00000293328.8:c.1045_1046insGC MANE Select	ENSP00000293328.3:p.Ala349GlyfsTer13
ENST00000293328.7:c.1045_1046insGC	ENSP00000293328.3:p.Ala349GlyfsTer13
ENST00000468312.1:n.1214_1215insGC
NM_012448.3:c.1045_1046insGC , LRG_192t1:c.1045_1046insGC	NP_036580.2:p.Ala349GlyfsTer13
XM_005257625.2:c.763_764insGC	XP_005257682.1:p.Ala255GlyfsTer13
XM_005257626.3:c.1045_1046insGC	XP_005257683.1:p.Ala349GlyfsTer13
XM_005257626.4:c.1045_1046insGC	XP_005257683.1:p.Ala349GlyfsTer13
XM_017024977.1:c.763_764insGC	XP_016880466.1:p.Ala255GlyfsTer13
XM_024450897.1:c.1045_1046insGC	XP_024306665.1:p.Ala349GlyfsTer13
XM_024450898.1:c.1045_1046insGC	XP_024306666.1:p.Ala349GlyfsTer13
NM_012448.4:c.1045_1046insGC MANE Select	NP_036580.2:p.Ala349GlyfsTer13