Canonical Allele Identifier: CA2637935746
Gene: STAT5B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42210089dup , CM000679.2:g.42210089dup GRCh38
NC_000017.10:g.40362107dup , CM000679.1:g.40362107dup GRCh37
NC_000017.9:g.37615633dup NCBI36
NG_007271.1:g.71318dup , LRG_192:g.71318dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000415845.2:c.1906+82dup ENSP00000398379.2:n.1906+82dup
ENST00000698774.1:n.2766+82dup
ENST00000698775.1:c.*1912+82dup ENSP00000513922.1:n.*1912+82dup
ENST00000698776.1:c.1906+82dup ENSP00000513923.1:n.1906+82dup
ENST00000698777.1:c.1906+82dup ENSP00000513924.1:n.1906+82dup
ENST00000698778.1:c.1906+82dup ENSP00000513925.1:n.1906+82dup
ENST00000698779.1:c.1906+82dup ENSP00000513926.1:n.1906+82dup
ENST00000698801.1:n.1777+82dup
ENST00000698802.1:c.1593+82dup ENSP00000513944.1:n.1593+82dup
ENST00000698803.1:c.*1651+82dup ENSP00000513945.1:n.*1651+82dup
ENST00000698804.1:n.4325+82dup
ENST00000698805.1:n.3249+82dup
ENST00000698806.1:c.*1620+82dup ENSP00000513946.1:n.*1620+82dup
ENST00000698807.1:n.3968+82dup
ENST00000698808.1:c.1903+82dup ENSP00000513947.1:n.1903+82dup
ENST00000698809.1:c.1813+82dup ENSP00000513948.1:n.1813+82dup
ENST00000698810.1:c.*1656+82dup ENSP00000513949.1:n.*1656+82dup
ENST00000698812.1:c.*1912+82dup ENSP00000513950.1:n.*1912+82dup
ENST00000698813.1:c.1906+82dup ENSP00000513951.1:n.1906+82dup
ENST00000698814.1:c.1906+82dup ENSP00000513952.1:n.1906+82dup
ENST00000698815.1:c.*54+256dup ENSP00000513953.1:n.*54+256dup
ENST00000293328.8:c.1906+82dup MANE Select ENSP00000293328.3:n.1906+82dup
ENST00000293328.7:c.1906+82dup ENSP00000293328.3:n.1906+82dup
ENST00000468496.5:n.750+82dup
ENST00000481253.2:n.321+82dup
NM_012448.3:c.1906+82dup , LRG_192t1:c.1906+82dup NP_036580.2:n.1906+82dup
XM_005257625.2:c.1624+82dup XP_005257682.1:n.1624+82dup
XM_017024977.1:c.1624+82dup XP_016880466.1:n.1624+82dup
XM_024450897.1:c.1906+82dup XP_024306665.1:n.1906+82dup
XM_024450898.1:c.1906+82dup XP_024306666.1:n.1906+82dup
NM_012448.4:c.1906+82dup MANE Select NP_036580.2:n.1906+82dup