Canonical Allele Identifier: CA772101997

Gene: STAT5A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42300657C>T , CM000679.2:g.42300657C>T	GRCh38
NC_000017.10:g.40452675C>T , CM000679.1:g.40452675C>T	GRCh37
NC_000017.9:g.37706201C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000590726.7:c.426-58C>T	ENSP00000464730.3:n.426-58C>T
ENST00000590949.6:c.834-58C>T MANE Select	ENSP00000468749.1:n.834-58C>T
ENST00000676585.1:c.834-58C>T	ENSP00000504449.1:n.834-58C>T
ENST00000676631.1:c.834-58C>T	ENSP00000503484.1:n.834-58C>T
ENST00000677301.1:c.834-58C>T	ENSP00000503262.1:n.834-58C>T
ENST00000677893.1:c.834-58C>T	ENSP00000504833.1:n.834-58C>T
ENST00000678903.1:c.783-58C>T	ENSP00000503304.1:n.783-58C>T
ENST00000345506.8:c.834-58C>T	ENSP00000341208.4:n.834-58C>T
ENST00000546010.6:c.744-58C>T	ENSP00000443107.1:n.744-58C>T
ENST00000588868.5:c.834-58C>T	ENSP00000465437.1:n.834-58C>T
ENST00000590949.5:c.834-58C>T	ENSP00000468749.1:n.834-58C>T
NM_001288718.1:c.834-58C>T	NP_001275647.1:n.834-58C>T
NM_001288719.1:c.744-58C>T	NP_001275648.1:n.744-58C>T
NM_001288720.1:c.834-58C>T	NP_001275649.1:n.834-58C>T
NM_003152.3:c.834-58C>T	NP_003143.2:n.834-58C>T
XM_005257624.2:c.834-58C>T	XP_005257681.1:n.834-58C>T
XM_005257624.3:c.834-58C>T	XP_005257681.1:n.834-58C>T
NM_001288718.2:c.834-58C>T MANE Select	NP_001275647.1:n.834-58C>T
NM_001288719.2:c.744-58C>T	NP_001275648.1:n.744-58C>T
NM_001288720.2:c.834-58C>T	NP_001275649.1:n.834-58C>T
NM_003152.4:c.834-58C>T	NP_003143.2:n.834-58C>T