Canonical Allele Identifier: CA399593688

Gene: STAT5B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42232037G>A , CM000679.2:g.42232037G>A	GRCh38
NC_000017.10:g.40384055G>A , CM000679.1:g.40384055G>A	GRCh37
NC_000017.9:g.37637581G>A	NCBI36
NG_007271.1:g.49370C>T , LRG_192:g.49370C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415845.2:c.91C>T	ENSP00000398379.2:p.Arg31Trp
ENST00000698774.1:n.265C>T
ENST00000698775.1:c.91C>T	ENSP00000513922.1:p.Arg31Trp
ENST00000698776.1:c.91C>T	ENSP00000513923.1:p.Arg31Trp
ENST00000698777.1:c.91C>T	ENSP00000513924.1:p.Arg31Trp
ENST00000698778.1:c.91C>T	ENSP00000513925.1:p.Arg31Trp
ENST00000698779.1:c.91C>T	ENSP00000513926.1:p.Arg31Trp
ENST00000698802.1:c.91C>T	ENSP00000513944.1:p.Arg31Trp
ENST00000698803.1:c.91C>T	ENSP00000513945.1:p.Arg31Trp
ENST00000698804.1:n.210C>T
ENST00000698805.1:n.212C>T
ENST00000698806.1:c.91C>T	ENSP00000513946.1:p.Arg31Trp
ENST00000698807.1:n.245C>T
ENST00000698808.1:c.91C>T	ENSP00000513947.1:p.Arg31Trp
ENST00000698809.1:c.91C>T	ENSP00000513948.1:p.Arg31Trp
ENST00000698810.1:c.91C>T	ENSP00000513949.1:p.Arg31Trp
ENST00000698812.1:c.91C>T	ENSP00000513950.1:p.Arg31Trp
ENST00000698813.1:c.91C>T	ENSP00000513951.1:p.Arg31Trp
ENST00000698814.1:c.91C>T	ENSP00000513952.1:p.Arg31Trp
ENST00000698815.1:c.91C>T	ENSP00000513953.1:p.Arg31Trp
ENST00000698816.1:n.179C>T
ENST00000698817.1:n.103C>T
ENST00000293328.8:c.91C>T MANE Select	ENSP00000293328.3:p.Arg31Trp
ENST00000293328.7:c.91C>T	ENSP00000293328.3:p.Arg31Trp
ENST00000415845.1:c.91C>T	ENSP00000398379.1:p.Arg31Trp
ENST00000468312.1:n.260C>T
NM_012448.3:c.91C>T , LRG_192t1:c.91C>T	NP_036580.2:p.Arg31Trp
XM_005257625.2:c.-35C>T	XP_005257682.1:n.-35C>T
XM_005257626.3:c.91C>T	XP_005257683.1:p.Arg31Trp
XM_005257626.4:c.91C>T	XP_005257683.1:p.Arg31Trp
XM_017024977.1:c.-35C>T	XP_016880466.1:n.-35C>T
XM_024450897.1:c.91C>T	XP_024306665.1:p.Arg31Trp
XM_024450898.1:c.91C>T	XP_024306666.1:p.Arg31Trp
NM_012448.4:c.91C>T MANE Select	NP_036580.2:p.Arg31Trp