Canonical Allele Identifier: CA2260379896
Gene: STAT5B HGNC NCBI

Linked Data

dbSNP Id: rs2080116429

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42210091del , CM000679.2:g.42210091del GRCh38
NC_000017.10:g.40362109del , CM000679.1:g.40362109del GRCh37
NC_000017.9:g.37615635del NCBI36
NG_007271.1:g.71317del , LRG_192:g.71317del

Transcript Alleles

HGVS Amino-acid Change
ENST00000415845.2:c.1906+81del ENSP00000398379.2:n.1906+81del
ENST00000698774.1:n.2766+81del
ENST00000698775.1:c.*1912+81del ENSP00000513922.1:n.*1912+81del
ENST00000698776.1:c.1906+81del ENSP00000513923.1:n.1906+81del
ENST00000698777.1:c.1906+81del ENSP00000513924.1:n.1906+81del
ENST00000698778.1:c.1906+81del ENSP00000513925.1:n.1906+81del
ENST00000698779.1:c.1906+81del ENSP00000513926.1:n.1906+81del
ENST00000698801.1:n.1777+81del
ENST00000698802.1:c.1593+81del ENSP00000513944.1:n.1593+81del
ENST00000698803.1:c.*1651+81del ENSP00000513945.1:n.*1651+81del
ENST00000698804.1:n.4325+81del
ENST00000698805.1:n.3249+81del
ENST00000698806.1:c.*1620+81del ENSP00000513946.1:n.*1620+81del
ENST00000698807.1:n.3968+81del
ENST00000698808.1:c.1903+81del ENSP00000513947.1:n.1903+81del
ENST00000698809.1:c.1813+81del ENSP00000513948.1:n.1813+81del
ENST00000698810.1:c.*1656+81del ENSP00000513949.1:n.*1656+81del
ENST00000698812.1:c.*1912+81del ENSP00000513950.1:n.*1912+81del
ENST00000698813.1:c.1906+81del ENSP00000513951.1:n.1906+81del
ENST00000698814.1:c.1906+81del ENSP00000513952.1:n.1906+81del
ENST00000698815.1:c.*54+255del ENSP00000513953.1:n.*54+255del
ENST00000293328.8:c.1906+81del MANE Select ENSP00000293328.3:n.1906+81del
ENST00000293328.7:c.1906+81del ENSP00000293328.3:n.1906+81del
ENST00000468496.5:n.750+81del
ENST00000481253.2:n.321+81del
NM_012448.3:c.1906+81del , LRG_192t1:c.1906+81del NP_036580.2:n.1906+81del
XM_005257625.2:c.1624+81del XP_005257682.1:n.1624+81del
XM_017024977.1:c.1624+81del XP_016880466.1:n.1624+81del
XM_024450897.1:c.1906+81del XP_024306665.1:n.1906+81del
XM_024450898.1:c.1906+81del XP_024306666.1:n.1906+81del
NM_012448.4:c.1906+81del MANE Select NP_036580.2:n.1906+81del