Canonical Allele Identifier: CA2500207634

Gene: STAT6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57095936C>T , CM000674.2:g.57095936C>T	GRCh38
NC_000012.11:g.57489719C>T , CM000674.1:g.57489719C>T	GRCh37
NC_000012.10:g.55775986C>T	NCBI36
NG_021272.1:g.20478G>A
NG_021272.2:g.41204G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000300134.8:c.*636G>A MANE Select	ENSP00000300134.3:n.*636G>A
ENST00000553533.2:c.*636G>A	ENSP00000451546.2:n.*636G>A
ENST00000554764.6:c.*2924G>A	ENSP00000451909.1:n.*2924G>A
ENST00000651176.1:c.*970G>A	ENSP00000498693.1:n.*970G>A
ENST00000300134.7:c.*636G>A	ENSP00000300134.3:n.*636G>A
ENST00000555222.5:n.2153G>A
NM_001178078.1:c.*636G>A	NP_001171549.1:n.*636G>A
NM_001178079.1:c.*636G>A	NP_001171550.1:n.*636G>A
NM_001178080.1:c.*636G>A	NP_001171551.1:n.*636G>A
NM_001178081.1:c.*636G>A	NP_001171552.1:n.*636G>A
NM_003153.4:c.*636G>A	NP_003144.3:n.*636G>A
NR_033659.1:n.3347G>A
XM_006719574.1:c.*636G>A	XP_006719637.1:n.*636G>A
XM_006719575.1:c.*636G>A	XP_006719638.1:n.*636G>A
XM_011538703.1:c.*636G>A	XP_011537005.1:n.*636G>A
XM_011538704.1:c.*636G>A	XP_011537006.1:n.*636G>A
XM_011538705.1:c.*636G>A	XP_011537007.1:n.*636G>A
XM_011538706.1:c.*636G>A	XP_011537008.1:n.*636G>A
XM_011538707.1:c.*636G>A	XP_011537009.1:n.*636G>A
XM_011538708.1:c.*636G>A	XP_011537010.1:n.*636G>A
XM_011538709.1:c.*636G>A	XP_011537011.1:n.*636G>A
XM_011538703.3:c.*636G>A	XP_011537005.1:n.*636G>A
XM_011538704.3:c.*636G>A	XP_011537006.1:n.*636G>A
XM_011538705.3:c.*636G>A	XP_011537007.1:n.*636G>A
XM_011538707.3:c.*636G>A	XP_011537009.1:n.*636G>A
XM_011538708.3:c.*636G>A	XP_011537010.1:n.*636G>A
NM_003153.5:c.*636G>A MANE Select	NP_003144.3:n.*636G>A
NM_001178078.2:c.*636G>A	NP_001171549.1:n.*636G>A
NM_001178079.2:c.*636G>A	NP_001171550.1:n.*636G>A
NM_001178080.2:c.*636G>A	NP_001171551.1:n.*636G>A
NM_001178081.2:c.*636G>A	NP_001171552.1:n.*636G>A
NR_033659.2:n.3296G>A