Canonical Allele Identifier: CA2254348251
Gene: FOXN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28534672G= , CM000679.2:g.28534672G= GRCh38
NC_000017.10:g.26861690G= , CM000679.1:g.26861690G= GRCh37
NC_000017.9:g.23885817G= NCBI36
NG_007260.1:g.15732G= , LRG_61:g.15732G=

Transcript Alleles

HGVS Amino-acid change
ENST00000577936.2:c.1136-35G= ENSP00000462159.2:n.1136-35G=
ENST00000579795.6:c.1136-35G= MANE Select ENSP00000464645.1:n.1136-35G=
ENST00000226247.2:c.1136-35G= ENSP00000226247.2:n.1136-35G=
ENST00000481916.6:c.*1195+69379C= ENSP00000436369.2:n.*1195+69379C=
ENST00000579795.5:c.1136-35G= ENSP00000464645.1:n.1136-35G=
NM_003593.2:c.1136-35G= , LRG_61t1:c.1136-35G= NP_003584.2:n.1136-35G=
XM_005258046.3:c.1136-35G= XP_005258103.1:n.1136-35G=
XM_011525354.1:c.1193-35G= XP_011523656.1:n.1193-35G=
XM_011525355.1:c.1190-35G= XP_011523657.1:n.1190-35G=
XM_011525356.1:c.1190-35G= XP_011523658.1:n.1190-35G=
XM_011525357.1:c.1172-35G= XP_011523659.1:n.1172-35G=
XM_011525358.1:c.1139-35G= XP_011523660.1:n.1139-35G=
XM_011525359.1:c.1139-35G= XP_011523661.1:n.1139-35G=
XM_011525360.1:c.1139-35G= XP_011523662.1:n.1139-35G=
XM_011525361.1:c.1136-35G= XP_011523663.1:n.1136-35G=
XM_011525362.1:c.1136-35G= XP_011523664.1:n.1136-35G=
XM_011525363.1:c.1192+134G= XP_011523665.1:n.1192+134G=
XM_011525364.1:c.671-35G= XP_011523666.1:n.671-35G=
XM_011525365.1:c.1192+134G= XP_011523667.1:n.1192+134G=
XM_011525366.1:c.593-35G= XP_011523668.1:n.593-35G=
XM_011525367.1:c.578-35G= XP_011523669.1:n.578-35G=
XM_011525368.1:c.500-35G= XP_011523670.1:n.500-35G=
XM_011525369.1:c.500-35G= XP_011523671.1:n.500-35G=
XM_011525370.1:c.500-35G= XP_011523672.1:n.500-35G=
XM_011525368.2:c.500-35G= XP_011523670.1:n.500-35G=
XM_011525369.2:c.500-35G= XP_011523671.1:n.500-35G=
XM_011525370.2:c.500-35G= XP_011523672.1:n.500-35G=
XM_017025228.1:c.1136-35G= XP_016880717.1:n.1136-35G=
XM_017025229.1:c.1138+134G= XP_016880718.1:n.1138+134G=
XM_017025230.1:c.1138+134G= XP_016880719.1:n.1138+134G=
XM_017025231.1:c.1138+134G= XP_016880720.1:n.1138+134G=
NM_001369369.1:c.1136-35G= MANE Select NP_001356298.1:n.1136-35G=
NM_003593.3:c.1136-35G= NP_003584.2:n.1136-35G=