Canonical Allele Identifier: CA2038691369
Gene: STAT6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57095951G= , CM000674.2:g.57095951G= GRCh38
NC_000012.11:g.57489734G= , CM000674.1:g.57489734G= GRCh37
NC_000012.10:g.55776001G= NCBI36
NG_021272.1:g.20463C=
NG_021272.2:g.41189C=

Transcript Alleles

HGVS Amino-acid change
ENST00000300134.8:c.*621C= MANE Select ENSP00000300134.3:n.*621C=
ENST00000553533.2:c.*621C= ENSP00000451546.2:n.*621C=
ENST00000554764.6:c.*2909C= ENSP00000451909.1:n.*2909C=
ENST00000651176.1:c.*955C= ENSP00000498693.1:n.*955C=
ENST00000300134.7:c.*621C= ENSP00000300134.3:n.*621C=
ENST00000555222.5:n.2138C=
NM_001178078.1:c.*621C= NP_001171549.1:n.*621C=
NM_001178079.1:c.*621C= NP_001171550.1:n.*621C=
NM_001178080.1:c.*621C= NP_001171551.1:n.*621C=
NM_001178081.1:c.*621C= NP_001171552.1:n.*621C=
NM_003153.4:c.*621C= NP_003144.3:n.*621C=
NR_033659.1:n.3332C=
XM_006719574.1:c.*621C= XP_006719637.1:n.*621C=
XM_006719575.1:c.*621C= XP_006719638.1:n.*621C=
XM_011538703.1:c.*621C= XP_011537005.1:n.*621C=
XM_011538704.1:c.*621C= XP_011537006.1:n.*621C=
XM_011538705.1:c.*621C= XP_011537007.1:n.*621C=
XM_011538706.1:c.*621C= XP_011537008.1:n.*621C=
XM_011538707.1:c.*621C= XP_011537009.1:n.*621C=
XM_011538708.1:c.*621C= XP_011537010.1:n.*621C=
XM_011538709.1:c.*621C= XP_011537011.1:n.*621C=
XM_011538703.3:c.*621C= XP_011537005.1:n.*621C=
XM_011538704.3:c.*621C= XP_011537006.1:n.*621C=
XM_011538705.3:c.*621C= XP_011537007.1:n.*621C=
XM_011538707.3:c.*621C= XP_011537009.1:n.*621C=
XM_011538708.3:c.*621C= XP_011537010.1:n.*621C=
NM_003153.5:c.*621C= MANE Select NP_003144.3:n.*621C=
NM_001178078.2:c.*621C= NP_001171549.1:n.*621C=
NM_001178079.2:c.*621C= NP_001171550.1:n.*621C=
NM_001178080.2:c.*621C= NP_001171551.1:n.*621C=
NM_001178081.2:c.*621C= NP_001171552.1:n.*621C=
NR_033659.2:n.3281C=