Canonical Allele Identifier: CA399576651

Gene: STAT5B

Linked Data

• MyVariant Identifiers: chr17:g.40362216T>A (hg19) ; chr17:g.42210198T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42210198T>A , CM000679.2:g.42210198T>A	GRCh38
NC_000017.10:g.40362216T>A , CM000679.1:g.40362216T>A	GRCh37
NC_000017.9:g.37615742T>A	NCBI36
NG_007271.1:g.71209A>T , LRG_192:g.71209A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000415845.2:c.1879A>T	ENSP00000398379.2:p.Ile627Phe
ENST00000698774.1:n.2739A>T
ENST00000698775.1:c.*1885A>T	ENSP00000513922.1:n.*1885A>T
ENST00000698776.1:c.1879A>T	ENSP00000513923.1:p.Ile627Phe
ENST00000698777.1:c.1879A>T	ENSP00000513924.1:p.Ile627Phe
ENST00000698778.1:c.1879A>T	ENSP00000513925.1:p.Ile627Phe
ENST00000698779.1:c.1879A>T	ENSP00000513926.1:p.Ile627Phe
ENST00000698801.1:n.1750A>T
ENST00000698802.1:c.1566A>T	ENSP00000513944.1:n.1566A>T
ENST00000698803.1:c.*1624A>T	ENSP00000513945.1:n.*1624A>T
ENST00000698804.1:n.4298A>T
ENST00000698805.1:n.3222A>T
ENST00000698806.1:c.*1593A>T	ENSP00000513946.1:n.*1593A>T
ENST00000698807.1:n.3941A>T
ENST00000698808.1:c.1876A>T	ENSP00000513947.1:p.Ile626Phe
ENST00000698809.1:c.1786A>T	ENSP00000513948.1:p.Ile596Phe
ENST00000698810.1:c.*1629A>T	ENSP00000513949.1:n.*1629A>T
ENST00000698812.1:c.*1885A>T	ENSP00000513950.1:n.*1885A>T
ENST00000698813.1:c.1879A>T	ENSP00000513951.1:p.Ile627Phe
ENST00000698814.1:c.1879A>T	ENSP00000513952.1:p.Ile627Phe
ENST00000698815.1:c.*54+147A>T	ENSP00000513953.1:n.*54+147A>T
ENST00000293328.8:c.1879A>T MANE Select	ENSP00000293328.3:p.Ile627Phe
ENST00000293328.7:c.1879A>T	ENSP00000293328.3:p.Ile627Phe
ENST00000468496.5:n.723A>T
ENST00000481253.2:n.294A>T
NM_012448.3:c.1879A>T , LRG_192t1:c.1879A>T	NP_036580.2:p.Ile627Phe
XM_005257625.2:c.1597A>T	XP_005257682.1:p.Ile533Phe
XM_017024977.1:c.1597A>T	XP_016880466.1:p.Ile533Phe
XM_024450897.1:c.1879A>T	XP_024306665.1:p.Ile627Phe
XM_024450898.1:c.1879A>T	XP_024306666.1:p.Ile627Phe
NM_012448.4:c.1879A>T MANE Select	NP_036580.2:p.Ile627Phe