Canonical Allele Identifier: CA983809656

Gene: STAT5B

Linked Data

• gnomAD v3: 17-42262061-T-TGGGGGGGGGGGGGGGGGGGGGG
• gnomAD v4: 17-42262061-T-TGGGGGGGGGGGGGGGGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42262061_42262062insGGGGGGGGGGGGGGGGGGGGGG , CM000679.2:g.42262061_42262062insGGGGGGGGGGGGGGGGGGGGGG	GRCh38
NC_000017.10:g.40414079_40414080insGGGGGGGGGGGGGGGGGGGGGG , CM000679.1:g.40414079_40414080insGGGGGGGGGGGGGGGGGGGGGG	GRCh37
NC_000017.9:g.37667605_37667606insGGGGGGGGGGGGGGGGGGGGGG	NCBI36
NG_007271.1:g.19345_19346insCCCCCCCCCCCCCCCCCCCCCC , LRG_192:g.19345_19346insCCCCCCCCCCCCCCCCCCCCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000415845.2:c.-11+14566_-11+14567insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000398379.2:n.-11+14566_-11+14567in...
ENST00000698774.1:n.164+14186_164+14187insCCCCCCCCCCCCCCCCCCCCCC
ENST00000698775.1:c.-11+14186_-11+14187insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000513922.1:n.-11+14186_-11+14187in...
ENST00000698776.1:c.-11+25725_-11+25726insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000513923.1:n.-11+25725_-11+25726in...
ENST00000698777.1:c.-11+26398_-11+26399insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000513924.1:n.-11+26398_-11+26399in...
ENST00000698778.1:c.-11+14186_-11+14187insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000513925.1:n.-11+14186_-11+14187in...
ENST00000698779.1:c.-11+14186_-11+14187insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000513926.1:n.-11+14186_-11+14187in...
ENST00000698803.1:c.-11+14186_-11+14187insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000513945.1:n.-11+14186_-11+14187in...
ENST00000698804.1:n.109+14186_109+14187insCCCCCCCCCCCCCCCCCCCCCC
ENST00000698805.1:n.111+14186_111+14187insCCCCCCCCCCCCCCCCCCCCCC
ENST00000698806.1:c.-11+14186_-11+14187insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000513946.1:n.-11+14186_-11+14187in...
ENST00000698807.1:n.144+14186_144+14187insCCCCCCCCCCCCCCCCCCCCCC
ENST00000698808.1:c.-11+14186_-11+14187insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000513947.1:n.-11+14186_-11+14187in...
ENST00000698809.1:c.-11+14186_-11+14187insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000513948.1:n.-11+14186_-11+14187in...
ENST00000698810.1:c.-11+14186_-11+14187insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000513949.1:n.-11+14186_-11+14187in...
ENST00000698813.1:c.-11+14186_-11+14187insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000513951.1:n.-11+14186_-11+14187in...
ENST00000698814.1:c.-11+14186_-11+14187insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000513952.1:n.-11+14186_-11+14187in...
ENST00000698815.1:c.-11+14186_-11+14187insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000513953.1:n.-11+14186_-11+14187in...
ENST00000698816.1:n.78+14186_78+14187insCCCCCCCCCCCCCCCCCCCCCC
ENST00000293328.8:c.-11+14186_-11+14187insCCCCCCCCCCCCCCCCCCCCCC MANE Select	ENSP00000293328.3:n.-11+14186_-11+14187in...
ENST00000293328.7:c.-11+14186_-11+14187insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000293328.3:n.-11+14186_-11+14187in...
ENST00000415845.1:c.-11+14566_-11+14567insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000398379.1:n.-11+14566_-11+14567in...
ENST00000468312.1:n.159+14186_159+14187insCCCCCCCCCCCCCCCCCCCCCC
NM_012448.3:c.-11+14186_-11+14187insCCCCCCCCCCCCCCCCCCCCCC , LRG_192t1:c.-11+14186_-11+14187insCCCCCCCCCCCCCCCCCCCCCC	NP_036580.2:n.-11+14186_-11+14187insCCCCC...
XM_005257626.3:c.-11+14186_-11+14187insCCCCCCCCCCCCCCCCCCCCCC	XP_005257683.1:n.-11+14186_-11+14187insCC...
XM_005257626.4:c.-11+14186_-11+14187insCCCCCCCCCCCCCCCCCCCCCC	XP_005257683.1:n.-11+14186_-11+14187insCC...
XM_017024977.1:c.-136+14186_-136+14187insCCCCCCCCCCCCCCCCCCCCCC	XP_016880466.1:n.-136+14186_-136+14187ins...
XM_024450897.1:c.-11+25725_-11+25726insCCCCCCCCCCCCCCCCCCCCCC	XP_024306665.1:n.-11+25725_-11+25726insCC...
XM_024450898.1:c.-11+6224_-11+6225insCCCCCCCCCCCCCCCCCCCCCC	XP_024306666.1:n.-11+6224_-11+6225insCCCC...
NM_012448.4:c.-11+14186_-11+14187insCCCCCCCCCCCCCCCCCCCCCC MANE Select	NP_036580.2:n.-11+14186_-11+14187insCCCCC...