Canonical Allele Identifier: CA2038691322
Gene: STAT6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57095927G= , CM000674.2:g.57095927G= GRCh38
NC_000012.11:g.57489710G= , CM000674.1:g.57489710G= GRCh37
NC_000012.10:g.55775977G= NCBI36
NG_021272.1:g.20487C=
NG_021272.2:g.41213C=

Transcript Alleles

HGVS Amino-acid change
ENST00000300134.8:c.*645C= MANE Select ENSP00000300134.3:n.*645C=
ENST00000553533.2:c.*645C= ENSP00000451546.2:n.*645C=
ENST00000554764.6:c.*2933C= ENSP00000451909.1:n.*2933C=
ENST00000651176.1:c.*979C= ENSP00000498693.1:n.*979C=
ENST00000300134.7:c.*645C= ENSP00000300134.3:n.*645C=
ENST00000555222.5:n.2162C=
NM_001178078.1:c.*645C= NP_001171549.1:n.*645C=
NM_001178079.1:c.*645C= NP_001171550.1:n.*645C=
NM_001178080.1:c.*645C= NP_001171551.1:n.*645C=
NM_001178081.1:c.*645C= NP_001171552.1:n.*645C=
NM_003153.4:c.*645C= NP_003144.3:n.*645C=
NR_033659.1:n.3356C=
XM_006719574.1:c.*645C= XP_006719637.1:n.*645C=
XM_006719575.1:c.*645C= XP_006719638.1:n.*645C=
XM_011538703.1:c.*645C= XP_011537005.1:n.*645C=
XM_011538704.1:c.*645C= XP_011537006.1:n.*645C=
XM_011538705.1:c.*645C= XP_011537007.1:n.*645C=
XM_011538706.1:c.*645C= XP_011537008.1:n.*645C=
XM_011538707.1:c.*645C= XP_011537009.1:n.*645C=
XM_011538708.1:c.*645C= XP_011537010.1:n.*645C=
XM_011538709.1:c.*645C= XP_011537011.1:n.*645C=
XM_011538703.3:c.*645C= XP_011537005.1:n.*645C=
XM_011538704.3:c.*645C= XP_011537006.1:n.*645C=
XM_011538705.3:c.*645C= XP_011537007.1:n.*645C=
XM_011538707.3:c.*645C= XP_011537009.1:n.*645C=
XM_011538708.3:c.*645C= XP_011537010.1:n.*645C=
NM_003153.5:c.*645C= MANE Select NP_003144.3:n.*645C=
NM_001178078.2:c.*645C= NP_001171549.1:n.*645C=
NM_001178079.2:c.*645C= NP_001171550.1:n.*645C=
NM_001178080.2:c.*645C= NP_001171551.1:n.*645C=
NM_001178081.2:c.*645C= NP_001171552.1:n.*645C=
NR_033659.2:n.3305C=