Canonical Allele Identifier: CA399576612

Gene: STAT5B

Linked Data

• MyVariant Identifiers: chr17:g.40362208A>C (hg19) ; chr17:g.42210190A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42210190A>C , CM000679.2:g.42210190A>C	GRCh38
NC_000017.10:g.40362208A>C , CM000679.1:g.40362208A>C	GRCh37
NC_000017.9:g.37615734A>C	NCBI36
NG_007271.1:g.71217T>G , LRG_192:g.71217T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000415845.2:c.1887T>G	ENSP00000398379.2:p.Ile629Met
ENST00000698774.1:n.2747T>G
ENST00000698775.1:c.*1893T>G	ENSP00000513922.1:n.*1893T>G
ENST00000698776.1:c.1887T>G	ENSP00000513923.1:p.Ile629Met
ENST00000698777.1:c.1887T>G	ENSP00000513924.1:p.Ile629Met
ENST00000698778.1:c.1887T>G	ENSP00000513925.1:p.Ile629Met
ENST00000698779.1:c.1887T>G	ENSP00000513926.1:p.Ile629Met
ENST00000698801.1:n.1758T>G
ENST00000698802.1:c.1574T>G	ENSP00000513944.1:n.1574T>G
ENST00000698803.1:c.*1632T>G	ENSP00000513945.1:n.*1632T>G
ENST00000698804.1:n.4306T>G
ENST00000698805.1:n.3230T>G
ENST00000698806.1:c.*1601T>G	ENSP00000513946.1:n.*1601T>G
ENST00000698807.1:n.3949T>G
ENST00000698808.1:c.1884T>G	ENSP00000513947.1:p.Ile628Met
ENST00000698809.1:c.1794T>G	ENSP00000513948.1:p.Ile598Met
ENST00000698810.1:c.*1637T>G	ENSP00000513949.1:n.*1637T>G
ENST00000698812.1:c.*1893T>G	ENSP00000513950.1:n.*1893T>G
ENST00000698813.1:c.1887T>G	ENSP00000513951.1:p.Ile629Met
ENST00000698814.1:c.1887T>G	ENSP00000513952.1:p.Ile629Met
ENST00000698815.1:c.*54+155T>G	ENSP00000513953.1:n.*54+155T>G
ENST00000293328.8:c.1887T>G MANE Select	ENSP00000293328.3:p.Ile629Met
ENST00000293328.7:c.1887T>G	ENSP00000293328.3:p.Ile629Met
ENST00000468496.5:n.731T>G
ENST00000481253.2:n.302T>G
NM_012448.3:c.1887T>G , LRG_192t1:c.1887T>G	NP_036580.2:p.Ile629Met
XM_005257625.2:c.1605T>G	XP_005257682.1:p.Ile535Met
XM_017024977.1:c.1605T>G	XP_016880466.1:p.Ile535Met
XM_024450897.1:c.1887T>G	XP_024306665.1:p.Ile629Met
XM_024450898.1:c.1887T>G	XP_024306666.1:p.Ile629Met
NM_012448.4:c.1887T>G MANE Select	NP_036580.2:p.Ile629Met