Canonical Allele Identifier: CA2260402944
Gene: STAT5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42261944_42261945delinsTC , CM000679.2:g.42261944_42261945delinsTC GRCh38
NC_000017.10:g.40413962_40413963delinsTC , CM000679.1:g.40413962_40413963delinsTC GRCh37
NC_000017.9:g.37667488_37667489delinsTC NCBI36
NG_007271.1:g.19462_19463delinsGA , LRG_192:g.19462_19463delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000415845.2:c.-11+14683_-11+14684delinsGA ENSP00000398379.2:n.-11+14683_-11+14684delinsGA
ENST00000698774.1:n.164+14303_164+14304delinsGA
ENST00000698775.1:c.-11+14303_-11+14304delinsGA ENSP00000513922.1:n.-11+14303_-11+14304delinsGA
ENST00000698776.1:c.-11+25842_-11+25843delinsGA ENSP00000513923.1:n.-11+25842_-11+25843delinsGA
ENST00000698777.1:c.-11+26515_-11+26516delinsGA ENSP00000513924.1:n.-11+26515_-11+26516delinsGA
ENST00000698778.1:c.-11+14303_-11+14304delinsGA ENSP00000513925.1:n.-11+14303_-11+14304delinsGA
ENST00000698779.1:c.-11+14303_-11+14304delinsGA ENSP00000513926.1:n.-11+14303_-11+14304delinsGA
ENST00000698803.1:c.-11+14303_-11+14304delinsGA ENSP00000513945.1:n.-11+14303_-11+14304delinsGA
ENST00000698804.1:n.109+14303_109+14304delinsGA
ENST00000698805.1:n.111+14303_111+14304delinsGA
ENST00000698806.1:c.-11+14303_-11+14304delinsGA ENSP00000513946.1:n.-11+14303_-11+14304delinsGA
ENST00000698807.1:n.144+14303_144+14304delinsGA
ENST00000698808.1:c.-11+14303_-11+14304delinsGA ENSP00000513947.1:n.-11+14303_-11+14304delinsGA
ENST00000698809.1:c.-11+14303_-11+14304delinsGA ENSP00000513948.1:n.-11+14303_-11+14304delinsGA
ENST00000698810.1:c.-11+14303_-11+14304delinsGA ENSP00000513949.1:n.-11+14303_-11+14304delinsGA
ENST00000698813.1:c.-11+14303_-11+14304delinsGA ENSP00000513951.1:n.-11+14303_-11+14304delinsGA
ENST00000698814.1:c.-11+14303_-11+14304delinsGA ENSP00000513952.1:n.-11+14303_-11+14304delinsGA
ENST00000698815.1:c.-11+14303_-11+14304delinsGA ENSP00000513953.1:n.-11+14303_-11+14304delinsGA
ENST00000698816.1:n.78+14303_78+14304delinsGA
ENST00000293328.8:c.-11+14303_-11+14304delinsGA MANE Select ENSP00000293328.3:n.-11+14303_-11+14304delinsGA
ENST00000293328.7:c.-11+14303_-11+14304delinsGA ENSP00000293328.3:n.-11+14303_-11+14304delinsGA
ENST00000415845.1:c.-11+14683_-11+14684delinsGA ENSP00000398379.1:n.-11+14683_-11+14684delinsGA
ENST00000468312.1:n.159+14303_159+14304delinsGA
NM_012448.3:c.-11+14303_-11+14304delinsGA , LRG_192t1:c.-11+14303_-11+14304delinsGA NP_036580.2:n.-11+14303_-11+14304delinsGA
XM_005257626.3:c.-11+14303_-11+14304delinsGA XP_005257683.1:n.-11+14303_-11+14304delinsGA
XM_005257626.4:c.-11+14303_-11+14304delinsGA XP_005257683.1:n.-11+14303_-11+14304delinsGA
XM_017024977.1:c.-136+14303_-136+14304delinsGA XP_016880466.1:n.-136+14303_-136+14304delinsGA
XM_024450897.1:c.-11+25842_-11+25843delinsGA XP_024306665.1:n.-11+25842_-11+25843delinsGA
XM_024450898.1:c.-11+6341_-11+6342delinsGA XP_024306666.1:n.-11+6341_-11+6342delinsGA
NM_012448.4:c.-11+14303_-11+14304delinsGA MANE Select NP_036580.2:n.-11+14303_-11+14304delinsGA