Canonical Allele Identifier: CA2038691343
Gene: STAT6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57095942C= , CM000674.2:g.57095942C= GRCh38
NC_000012.11:g.57489725C= , CM000674.1:g.57489725C= GRCh37
NC_000012.10:g.55775992C= NCBI36
NG_021272.1:g.20472G=
NG_021272.2:g.41198G=

Transcript Alleles

HGVS Amino-acid change
ENST00000300134.8:c.*630G= MANE Select ENSP00000300134.3:n.*630G=
ENST00000553533.2:c.*630G= ENSP00000451546.2:n.*630G=
ENST00000554764.6:c.*2918G= ENSP00000451909.1:n.*2918G=
ENST00000651176.1:c.*964G= ENSP00000498693.1:n.*964G=
ENST00000300134.7:c.*630G= ENSP00000300134.3:n.*630G=
ENST00000555222.5:n.2147G=
NM_001178078.1:c.*630G= NP_001171549.1:n.*630G=
NM_001178079.1:c.*630G= NP_001171550.1:n.*630G=
NM_001178080.1:c.*630G= NP_001171551.1:n.*630G=
NM_001178081.1:c.*630G= NP_001171552.1:n.*630G=
NM_003153.4:c.*630G= NP_003144.3:n.*630G=
NR_033659.1:n.3341G=
XM_006719574.1:c.*630G= XP_006719637.1:n.*630G=
XM_006719575.1:c.*630G= XP_006719638.1:n.*630G=
XM_011538703.1:c.*630G= XP_011537005.1:n.*630G=
XM_011538704.1:c.*630G= XP_011537006.1:n.*630G=
XM_011538705.1:c.*630G= XP_011537007.1:n.*630G=
XM_011538706.1:c.*630G= XP_011537008.1:n.*630G=
XM_011538707.1:c.*630G= XP_011537009.1:n.*630G=
XM_011538708.1:c.*630G= XP_011537010.1:n.*630G=
XM_011538709.1:c.*630G= XP_011537011.1:n.*630G=
XM_011538703.3:c.*630G= XP_011537005.1:n.*630G=
XM_011538704.3:c.*630G= XP_011537006.1:n.*630G=
XM_011538705.3:c.*630G= XP_011537007.1:n.*630G=
XM_011538707.3:c.*630G= XP_011537009.1:n.*630G=
XM_011538708.3:c.*630G= XP_011537010.1:n.*630G=
NM_003153.5:c.*630G= MANE Select NP_003144.3:n.*630G=
NM_001178078.2:c.*630G= NP_001171549.1:n.*630G=
NM_001178079.2:c.*630G= NP_001171550.1:n.*630G=
NM_001178080.2:c.*630G= NP_001171551.1:n.*630G=
NM_001178081.2:c.*630G= NP_001171552.1:n.*630G=
NR_033659.2:n.3290G=