Canonical Allele Identifier: CA500059826

Gene: STAT5B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42218264C>A , CM000679.2:g.42218264C>A	GRCh38
NC_000017.10:g.40370282C>A , CM000679.1:g.40370282C>A	GRCh37
NC_000017.9:g.37623808C>A	NCBI36
NG_007271.1:g.63143G>T , LRG_192:g.63143G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_012448.4:c.1056G>T MANE Select	NP_036580.2:p.Val352=
ENST00000293328.8:c.1056G>T MANE Select	ENSP00000293328.3:p.Val352=
NM_012448.3:c.1056G>T , LRG_192t1:c.1056G>T	NP_036580.2:p.Val352=
ENST00000293328.7:c.1056G>T	ENSP00000293328.3:p.Val352=
ENST00000415845.2:c.1056G>T	ENSP00000398379.2:p.Val352=
ENST00000468312.1:n.1225G>T
ENST00000698774.1:n.1230G>T
ENST00000698775.1:c.*1062G>T	ENSP00000513922.1:n.*1062G>T
ENST00000698776.1:c.1056G>T	ENSP00000513923.1:p.Val352=
ENST00000698777.1:c.1056G>T	ENSP00000513924.1:p.Val352=
ENST00000698778.1:c.1056G>T	ENSP00000513925.1:p.Val352=
ENST00000698779.1:c.1056G>T	ENSP00000513926.1:p.Val352=
ENST00000698801.1:n.932G>T
ENST00000698802.1:c.743G>T	ENSP00000513944.1:n.743G>T
ENST00000698803.1:c.*806G>T	ENSP00000513945.1:n.*806G>T
ENST00000698804.1:n.2789G>T
ENST00000698805.1:n.2399G>T
ENST00000698806.1:c.*770G>T	ENSP00000513946.1:n.*770G>T
ENST00000698807.1:n.2432G>T
ENST00000698808.1:c.1053G>T	ENSP00000513947.1:p.Val351=
ENST00000698809.1:c.1056G>T	ENSP00000513948.1:p.Val352=
ENST00000698810.1:c.*806G>T	ENSP00000513949.1:n.*806G>T
ENST00000698812.1:c.*1062G>T	ENSP00000513950.1:n.*1062G>T
ENST00000698813.1:c.1056G>T	ENSP00000513951.1:p.Val352=
ENST00000698814.1:c.1056G>T	ENSP00000513952.1:p.Val352=
ENST00000698815.1:c.1056G>T	ENSP00000513953.1:p.Val352=
ENST00000698816.1:n.1144G>T
XM_005257625.2:c.774G>T	XP_005257682.1:p.Val258=
XM_005257626.3:c.1056G>T	XP_005257683.1:p.Val352=
XM_005257626.4:c.1056G>T	XP_005257683.1:p.Val352=
XM_017024977.1:c.774G>T	XP_016880466.1:p.Val258=
XM_024450897.1:c.1056G>T	XP_024306665.1:p.Val352=
XM_024450898.1:c.1056G>T	XP_024306666.1:p.Val352=