Canonical Allele Identifier: CA16620350
Gene: FOXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 422253
dbSNP Id: rs1064795660

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28534539_28534540delinsAG , CM000679.2:g.28534539_28534540delinsAG GRCh38
NC_000017.10:g.26861557_26861558delinsAG , CM000679.1:g.26861557_26861558delinsAG GRCh37
NC_000017.9:g.23885684_23885685delinsAG NCBI36
NG_007260.1:g.15599_15600delinsAG , LRG_61:g.15599_15600delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000577936.2:c.1135+1_1135+2delinsAG ENSP00000462159.2:n.1135+1_1135+2delinsAG...
ENST00000579795.6:c.1135+1_1135+2delinsAG MANE Select ENSP00000464645.1:n.1135+1_1135+2delinsAG...
ENST00000226247.2:c.1135+1_1135+2delinsAG ENSP00000226247.2:n.1135+1_1135+2delinsAG...
ENST00000481916.6:c.*1195+69511_*1195+69512delinsCT ENSP00000436369.2:n.*1195+69511_*1195+695...
ENST00000579795.5:c.1135+1_1135+2delinsAG ENSP00000464645.1:n.1135+1_1135+2delinsAG...
NM_003593.2:c.1135+1_1135+2delinsAG , LRG_61t1:c.1135+1_1135+2delinsAG NP_003584.2:n.1135+1_1135+2delinsAG
XM_005258046.3:c.1135+1_1135+2delinsAG XP_005258103.1:n.1135+1_1135+2delinsAG
XM_011525354.1:c.1192+1_1192+2delinsAG XP_011523656.1:n.1192+1_1192+2delinsAG
XM_011525355.1:c.1189+1_1189+2delinsAG XP_011523657.1:n.1189+1_1189+2delinsAG
XM_011525356.1:c.1189+1_1189+2delinsAG XP_011523658.1:n.1189+1_1189+2delinsAG
XM_011525357.1:c.1171+1_1171+2delinsAG XP_011523659.1:n.1171+1_1171+2delinsAG
XM_011525358.1:c.1138+1_1138+2delinsAG XP_011523660.1:n.1138+1_1138+2delinsAG
XM_011525359.1:c.1138+1_1138+2delinsAG XP_011523661.1:n.1138+1_1138+2delinsAG
XM_011525360.1:c.1138+1_1138+2delinsAG XP_011523662.1:n.1138+1_1138+2delinsAG
XM_011525361.1:c.1135+1_1135+2delinsAG XP_011523663.1:n.1135+1_1135+2delinsAG
XM_011525362.1:c.1135+1_1135+2delinsAG XP_011523664.1:n.1135+1_1135+2delinsAG
XM_011525363.1:c.1192+1_1192+2delinsAG XP_011523665.1:n.1192+1_1192+2delinsAG
XM_011525364.1:c.670+1_670+2delinsAG XP_011523666.1:n.670+1_670+2delinsAG
XM_011525365.1:c.1192+1_1192+2delinsAG XP_011523667.1:n.1192+1_1192+2delinsAG
XM_011525366.1:c.592+1_592+2delinsAG XP_011523668.1:n.592+1_592+2delinsAG
XM_011525367.1:c.577+1_577+2delinsAG XP_011523669.1:n.577+1_577+2delinsAG
XM_011525368.1:c.499+1_499+2delinsAG XP_011523670.1:n.499+1_499+2delinsAG
XM_011525369.1:c.499+1_499+2delinsAG XP_011523671.1:n.499+1_499+2delinsAG
XM_011525370.1:c.499+1_499+2delinsAG XP_011523672.1:n.499+1_499+2delinsAG
XM_011525368.2:c.499+1_499+2delinsAG XP_011523670.1:n.499+1_499+2delinsAG
XM_011525369.2:c.499+1_499+2delinsAG XP_011523671.1:n.499+1_499+2delinsAG
XM_011525370.2:c.499+1_499+2delinsAG XP_011523672.1:n.499+1_499+2delinsAG
XM_017025228.1:c.1135+1_1135+2delinsAG XP_016880717.1:n.1135+1_1135+2delinsAG
XM_017025229.1:c.1138+1_1138+2delinsAG XP_016880718.1:n.1138+1_1138+2delinsAG
XM_017025230.1:c.1138+1_1138+2delinsAG XP_016880719.1:n.1138+1_1138+2delinsAG
XM_017025231.1:c.1138+1_1138+2delinsAG XP_016880720.1:n.1138+1_1138+2delinsAG
NM_001369369.1:c.1135+1_1135+2delinsAG MANE Select NP_001356298.1:n.1135+1_1135+2delinsAG
NM_003593.3:c.1135+1_1135+2delinsAG NP_003584.2:n.1135+1_1135+2delinsAG