Canonical Allele Identifier: CA2580601750

Gene: STAT6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57095926T>A , CM000674.2:g.57095926T>A	GRCh38
NC_000012.11:g.57489709T>A , CM000674.1:g.57489709T>A	GRCh37
NC_000012.10:g.55775976T>A	NCBI36
NG_021272.1:g.20488A>T
NG_021272.2:g.41214A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000300134.8:c.*646A>T MANE Select	ENSP00000300134.3:n.*646A>T
ENST00000553533.2:c.*646A>T	ENSP00000451546.2:n.*646A>T
ENST00000554764.6:c.*2934A>T	ENSP00000451909.1:n.*2934A>T
ENST00000651176.1:c.*980A>T	ENSP00000498693.1:n.*980A>T
ENST00000300134.7:c.*646A>T	ENSP00000300134.3:n.*646A>T
ENST00000555222.5:n.2163A>T
NM_001178078.1:c.*646A>T	NP_001171549.1:n.*646A>T
NM_001178079.1:c.*646A>T	NP_001171550.1:n.*646A>T
NM_001178080.1:c.*646A>T	NP_001171551.1:n.*646A>T
NM_001178081.1:c.*646A>T	NP_001171552.1:n.*646A>T
NM_003153.4:c.*646A>T	NP_003144.3:n.*646A>T
NR_033659.1:n.3357A>T
XM_006719574.1:c.*646A>T	XP_006719637.1:n.*646A>T
XM_006719575.1:c.*646A>T	XP_006719638.1:n.*646A>T
XM_011538703.1:c.*646A>T	XP_011537005.1:n.*646A>T
XM_011538704.1:c.*646A>T	XP_011537006.1:n.*646A>T
XM_011538705.1:c.*646A>T	XP_011537007.1:n.*646A>T
XM_011538706.1:c.*646A>T	XP_011537008.1:n.*646A>T
XM_011538707.1:c.*646A>T	XP_011537009.1:n.*646A>T
XM_011538708.1:c.*646A>T	XP_011537010.1:n.*646A>T
XM_011538709.1:c.*646A>T	XP_011537011.1:n.*646A>T
XM_011538703.3:c.*646A>T	XP_011537005.1:n.*646A>T
XM_011538704.3:c.*646A>T	XP_011537006.1:n.*646A>T
XM_011538705.3:c.*646A>T	XP_011537007.1:n.*646A>T
XM_011538707.3:c.*646A>T	XP_011537009.1:n.*646A>T
XM_011538708.3:c.*646A>T	XP_011537010.1:n.*646A>T
NM_003153.5:c.*646A>T MANE Select	NP_003144.3:n.*646A>T
NM_001178078.2:c.*646A>T	NP_001171549.1:n.*646A>T
NM_001178079.2:c.*646A>T	NP_001171550.1:n.*646A>T
NM_001178080.2:c.*646A>T	NP_001171551.1:n.*646A>T
NM_001178081.2:c.*646A>T	NP_001171552.1:n.*646A>T
NR_033659.2:n.3306A>T