Canonical Allele Identifier: CA2260424132

Gene: STAT5A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42307544A= , CM000679.2:g.42307544A=	GRCh38
NC_000017.10:g.40459562A= , CM000679.1:g.40459562A=	GRCh37
NC_000017.9:g.37713088A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001288718.2:c.1776-49A= MANE Select	NP_001275647.1:n.1776-49A=
ENST00000590949.6:c.1776-49A= MANE Select	ENSP00000468749.1:n.1776-49A=
NM_001288718.1:c.1776-49A=	NP_001275647.1:n.1776-49A=
NM_001288719.1:c.1686-49A=	NP_001275648.1:n.1686-49A=
NM_001288719.2:c.1686-49A=	NP_001275648.1:n.1686-49A=
NM_001288720.1:c.1683-49A=	NP_001275649.1:n.1683-49A=
NM_001288720.2:c.1683-49A=	NP_001275649.1:n.1683-49A=
NM_003152.3:c.1776-49A=	NP_003143.2:n.1776-49A=
NM_003152.4:c.1776-49A=	NP_003143.2:n.1776-49A=
ENST00000345506.8:c.1776-49A=	ENSP00000341208.4:n.1776-49A=
ENST00000468096.5:n.430-49A=
ENST00000546010.6:c.1686-49A=	ENSP00000443107.1:n.1686-49A=
ENST00000587646.1:c.240-49A=	ENSP00000466320.1:n.240-49A=
ENST00000587646.2:n.374-49A=
ENST00000588868.5:c.1683-49A=	ENSP00000465437.1:n.1683-49A=
ENST00000590726.7:c.1368-49A=	ENSP00000464730.3:n.1368-49A=
ENST00000590949.5:c.1776-49A=	ENSP00000468749.1:n.1776-49A=
ENST00000591556.1:n.428-49A=
ENST00000676585.1:c.1776-49A=	ENSP00000504449.1:n.1776-49A=
ENST00000676631.1:c.1776-49A=	ENSP00000503484.1:n.1776-49A=
ENST00000677301.1:c.1776-49A=	ENSP00000503262.1:n.1776-49A=
ENST00000677893.1:c.1770-49A=	ENSP00000504833.1:n.1770-49A=
ENST00000678903.1:c.1725-49A=	ENSP00000503304.1:n.1725-49A=
XM_005257624.2:c.1776-49A=	XP_005257681.1:n.1776-49A=
XM_005257624.3:c.1776-49A=	XP_005257681.1:n.1776-49A=