Canonical Allele Identifier: CA398323056
Gene: FOXN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28529136T>C , CM000679.2:g.28529136T>C GRCh38
NC_000017.10:g.26856154T>C , CM000679.1:g.26856154T>C GRCh37
NC_000017.9:g.23880281T>C NCBI36
NG_007260.1:g.10196T>C , LRG_61:g.10196T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000577936.2:c.742T>C ENSP00000462159.2:p.Ser248Pro
ENST00000579795.6:c.742T>C MANE Select ENSP00000464645.1:p.Ser248Pro
ENST00000226247.2:c.742T>C ENSP00000226247.2:p.Ser248Pro
ENST00000481916.6:c.*1196-73027A>G ENSP00000436369.2:n.*1196-73027A>G
ENST00000579795.5:c.742T>C ENSP00000464645.1:p.Ser248Pro
NM_003593.2:c.742T>C , LRG_61t1:c.742T>C NP_003584.2:p.Ser248Pro
XM_005258046.3:c.742T>C XP_005258103.1:p.Ser248Pro
XM_011525354.1:c.799T>C XP_011523656.1:p.Ser267Pro
XM_011525355.1:c.796T>C XP_011523657.1:p.Ser266Pro
XM_011525356.1:c.796T>C XP_011523658.1:p.Ser266Pro
XM_011525357.1:c.778T>C XP_011523659.1:p.Ser260Pro
XM_011525358.1:c.745T>C XP_011523660.1:p.Ser249Pro
XM_011525359.1:c.745T>C XP_011523661.1:p.Ser249Pro
XM_011525360.1:c.745T>C XP_011523662.1:p.Ser249Pro
XM_011525361.1:c.742T>C XP_011523663.1:p.Ser248Pro
XM_011525362.1:c.742T>C XP_011523664.1:p.Ser248Pro
XM_011525363.1:c.799T>C XP_011523665.1:p.Ser267Pro
XM_011525364.1:c.277T>C XP_011523666.1:p.Ser93Pro
XM_011525365.1:c.799T>C XP_011523667.1:p.Ser267Pro
XM_011525366.1:c.199T>C XP_011523668.1:p.Ser67Pro
XM_011525367.1:c.184T>C XP_011523669.1:p.Ser62Pro
XM_011525368.1:c.106T>C XP_011523670.1:p.Ser36Pro
XM_011525369.1:c.106T>C XP_011523671.1:p.Ser36Pro
XM_011525370.1:c.106T>C XP_011523672.1:p.Ser36Pro
XM_011525368.2:c.106T>C XP_011523670.1:p.Ser36Pro
XM_011525369.2:c.106T>C XP_011523671.1:p.Ser36Pro
XM_011525370.2:c.106T>C XP_011523672.1:p.Ser36Pro
XM_017025228.1:c.742T>C XP_016880717.1:p.Ser248Pro
XM_017025229.1:c.745T>C XP_016880718.1:p.Ser249Pro
XM_017025230.1:c.745T>C XP_016880719.1:p.Ser249Pro
XM_017025231.1:c.745T>C XP_016880720.1:p.Ser249Pro
NM_001369369.1:c.742T>C MANE Select NP_001356298.1:p.Ser248Pro
NM_003593.3:c.742T>C NP_003584.2:p.Ser248Pro