Canonical Allele Identifier: CA2796130500

Gene: STAT6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57095985G>A , CM000674.2:g.57095985G>A	GRCh38
NC_000012.11:g.57489768G>A , CM000674.1:g.57489768G>A	GRCh37
NC_000012.10:g.55776035G>A	NCBI36
NG_021272.1:g.20429C>T
NG_021272.2:g.41155C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300134.8:c.*587C>T MANE Select	ENSP00000300134.3:n.*587C>T
ENST00000553533.2:c.*587C>T	ENSP00000451546.2:n.*587C>T
ENST00000554764.6:c.*2875C>T	ENSP00000451909.1:n.*2875C>T
ENST00000651176.1:c.*921C>T	ENSP00000498693.1:n.*921C>T
ENST00000300134.7:c.*587C>T	ENSP00000300134.3:n.*587C>T
ENST00000555222.5:n.2104C>T
NM_001178078.1:c.*587C>T	NP_001171549.1:n.*587C>T
NM_001178079.1:c.*587C>T	NP_001171550.1:n.*587C>T
NM_001178080.1:c.*587C>T	NP_001171551.1:n.*587C>T
NM_001178081.1:c.*587C>T	NP_001171552.1:n.*587C>T
NM_003153.4:c.*587C>T	NP_003144.3:n.*587C>T
NR_033659.1:n.3298C>T
XM_006719574.1:c.*587C>T	XP_006719637.1:n.*587C>T
XM_006719575.1:c.*587C>T	XP_006719638.1:n.*587C>T
XM_011538703.1:c.*587C>T	XP_011537005.1:n.*587C>T
XM_011538704.1:c.*587C>T	XP_011537006.1:n.*587C>T
XM_011538705.1:c.*587C>T	XP_011537007.1:n.*587C>T
XM_011538706.1:c.*587C>T	XP_011537008.1:n.*587C>T
XM_011538707.1:c.*587C>T	XP_011537009.1:n.*587C>T
XM_011538708.1:c.*587C>T	XP_011537010.1:n.*587C>T
XM_011538709.1:c.*587C>T	XP_011537011.1:n.*587C>T
XM_011538703.3:c.*587C>T	XP_011537005.1:n.*587C>T
XM_011538704.3:c.*587C>T	XP_011537006.1:n.*587C>T
XM_011538705.3:c.*587C>T	XP_011537007.1:n.*587C>T
XM_011538707.3:c.*587C>T	XP_011537009.1:n.*587C>T
XM_011538708.3:c.*587C>T	XP_011537010.1:n.*587C>T
NM_003153.5:c.*587C>T MANE Select	NP_003144.3:n.*587C>T
NM_001178078.2:c.*587C>T	NP_001171549.1:n.*587C>T
NM_001178079.2:c.*587C>T	NP_001171550.1:n.*587C>T
NM_001178080.2:c.*587C>T	NP_001171551.1:n.*587C>T
NM_001178081.2:c.*587C>T	NP_001171552.1:n.*587C>T
NR_033659.2:n.3247C>T