Canonical Allele Identifier: CA2038691420

Gene: STAT6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57095983T= , CM000674.2:g.57095983T=	GRCh38
NC_000012.11:g.57489766T= , CM000674.1:g.57489766T=	GRCh37
NC_000012.10:g.55776033T=	NCBI36
NG_021272.1:g.20431A=
NG_021272.2:g.41157A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300134.8:c.*589A= MANE Select	ENSP00000300134.3:n.*589A=
ENST00000553533.2:c.*589A=	ENSP00000451546.2:n.*589A=
ENST00000554764.6:c.*2877A=	ENSP00000451909.1:n.*2877A=
ENST00000651176.1:c.*923A=	ENSP00000498693.1:n.*923A=
ENST00000300134.7:c.*589A=	ENSP00000300134.3:n.*589A=
ENST00000555222.5:n.2106A=
NM_001178078.1:c.*589A=	NP_001171549.1:n.*589A=
NM_001178079.1:c.*589A=	NP_001171550.1:n.*589A=
NM_001178080.1:c.*589A=	NP_001171551.1:n.*589A=
NM_001178081.1:c.*589A=	NP_001171552.1:n.*589A=
NM_003153.4:c.*589A=	NP_003144.3:n.*589A=
NR_033659.1:n.3300A=
XM_006719574.1:c.*589A=	XP_006719637.1:n.*589A=
XM_006719575.1:c.*589A=	XP_006719638.1:n.*589A=
XM_011538703.1:c.*589A=	XP_011537005.1:n.*589A=
XM_011538704.1:c.*589A=	XP_011537006.1:n.*589A=
XM_011538705.1:c.*589A=	XP_011537007.1:n.*589A=
XM_011538706.1:c.*589A=	XP_011537008.1:n.*589A=
XM_011538707.1:c.*589A=	XP_011537009.1:n.*589A=
XM_011538708.1:c.*589A=	XP_011537010.1:n.*589A=
XM_011538709.1:c.*589A=	XP_011537011.1:n.*589A=
XM_011538703.3:c.*589A=	XP_011537005.1:n.*589A=
XM_011538704.3:c.*589A=	XP_011537006.1:n.*589A=
XM_011538705.3:c.*589A=	XP_011537007.1:n.*589A=
XM_011538707.3:c.*589A=	XP_011537009.1:n.*589A=
XM_011538708.3:c.*589A=	XP_011537010.1:n.*589A=
NM_003153.5:c.*589A= MANE Select	NP_003144.3:n.*589A=
NM_001178078.2:c.*589A=	NP_001171549.1:n.*589A=
NM_001178079.2:c.*589A=	NP_001171550.1:n.*589A=
NM_001178080.2:c.*589A=	NP_001171551.1:n.*589A=
NM_001178081.2:c.*589A=	NP_001171552.1:n.*589A=
NR_033659.2:n.3249A=