Canonical Allele Identifier: CA2576273996

Gene: STAT5B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42218261_42218268del , CM000679.2:g.42218261_42218268del	GRCh38
NC_000017.10:g.40370279_40370286del , CM000679.1:g.40370279_40370286del	GRCh37
NC_000017.9:g.37623805_37623812del	NCBI36
NG_007271.1:g.63142_63149del , LRG_192:g.63142_63149del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415845.2:c.1055_1062del	ENSP00000398379.2:p.Val352AlafsTer22
ENST00000698774.1:n.1229_1236del
ENST00000698775.1:c.*1061_*1068del	ENSP00000513922.1:n.*1061_*1068del
ENST00000698776.1:c.1055_1062del	ENSP00000513923.1:p.Val352AlafsTer22
ENST00000698777.1:c.1055_1062del	ENSP00000513924.1:p.Val352AlafsTer22
ENST00000698778.1:c.1055_1062del	ENSP00000513925.1:p.Val352AlafsTer22
ENST00000698779.1:c.1055_1062del	ENSP00000513926.1:p.Val352AlafsTer22
ENST00000698801.1:n.931_938del
ENST00000698802.1:c.742_749del	ENSP00000513944.1:n.742_749del
ENST00000698803.1:c.*805_*812del	ENSP00000513945.1:n.*805_*812del
ENST00000698804.1:n.2788_2795del
ENST00000698805.1:n.2398_2405del
ENST00000698806.1:c.*769_*776del	ENSP00000513946.1:n.*769_*776del
ENST00000698807.1:n.2431_2438del
ENST00000698808.1:c.1052_1059del	ENSP00000513947.1:p.Val351AlafsTer22
ENST00000698809.1:c.1055_1062del	ENSP00000513948.1:p.Val352AlafsTer22
ENST00000698810.1:c.*805_*812del	ENSP00000513949.1:n.*805_*812del
ENST00000698812.1:c.*1061_*1068del	ENSP00000513950.1:n.*1061_*1068del
ENST00000698813.1:c.1055_1062del	ENSP00000513951.1:p.Val352AlafsTer22
ENST00000698814.1:c.1055_1062del	ENSP00000513952.1:p.Val352AlafsTer22
ENST00000698815.1:c.1055_1062del	ENSP00000513953.1:p.Val352AlafsTer22
ENST00000698816.1:n.1143_1150del
ENST00000293328.8:c.1055_1062del MANE Select	ENSP00000293328.3:p.Val352AlafsTer22
ENST00000293328.7:c.1055_1062del	ENSP00000293328.3:p.Val352AlafsTer22
ENST00000468312.1:n.1224_1231del
NM_012448.3:c.1055_1062del , LRG_192t1:c.1055_1062del	NP_036580.2:p.Val352AlafsTer22
XM_005257625.2:c.773_780del	XP_005257682.1:p.Val258AlafsTer22
XM_005257626.3:c.1055_1062del	XP_005257683.1:p.Val352AlafsTer22
XM_005257626.4:c.1055_1062del	XP_005257683.1:p.Val352AlafsTer22
XM_017024977.1:c.773_780del	XP_016880466.1:p.Val258AlafsTer22
XM_024450897.1:c.1055_1062del	XP_024306665.1:p.Val352AlafsTer22
XM_024450898.1:c.1055_1062del	XP_024306666.1:p.Val352AlafsTer22
NM_012448.4:c.1055_1062del MANE Select	NP_036580.2:p.Val352AlafsTer22