Canonical Allele Identifier: CA398323132
Gene: FOXN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28529155A>G , CM000679.2:g.28529155A>G GRCh38
NC_000017.10:g.26856173A>G , CM000679.1:g.26856173A>G GRCh37
NC_000017.9:g.23880300A>G NCBI36
NG_007260.1:g.10215A>G , LRG_61:g.10215A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000577936.2:c.761A>G ENSP00000462159.2:p.Gln254Arg
ENST00000579795.6:c.761A>G MANE Select ENSP00000464645.1:p.Gln254Arg
ENST00000226247.2:c.761A>G ENSP00000226247.2:p.Gln254Arg
ENST00000481916.6:c.*1196-73046T>C ENSP00000436369.2:n.*1196-73046T>C
ENST00000579795.5:c.761A>G ENSP00000464645.1:p.Gln254Arg
NM_003593.2:c.761A>G , LRG_61t1:c.761A>G NP_003584.2:p.Gln254Arg
XM_005258046.3:c.761A>G XP_005258103.1:p.Gln254Arg
XM_011525354.1:c.818A>G XP_011523656.1:p.Gln273Arg
XM_011525355.1:c.815A>G XP_011523657.1:p.Gln272Arg
XM_011525356.1:c.815A>G XP_011523658.1:p.Gln272Arg
XM_011525357.1:c.797A>G XP_011523659.1:p.Gln266Arg
XM_011525358.1:c.764A>G XP_011523660.1:p.Gln255Arg
XM_011525359.1:c.764A>G XP_011523661.1:p.Gln255Arg
XM_011525360.1:c.764A>G XP_011523662.1:p.Gln255Arg
XM_011525361.1:c.761A>G XP_011523663.1:p.Gln254Arg
XM_011525362.1:c.761A>G XP_011523664.1:p.Gln254Arg
XM_011525363.1:c.818A>G XP_011523665.1:p.Gln273Arg
XM_011525364.1:c.296A>G XP_011523666.1:p.Gln99Arg
XM_011525365.1:c.818A>G XP_011523667.1:p.Gln273Arg
XM_011525366.1:c.218A>G XP_011523668.1:p.Gln73Arg
XM_011525367.1:c.203A>G XP_011523669.1:p.Gln68Arg
XM_011525368.1:c.125A>G XP_011523670.1:p.Gln42Arg
XM_011525369.1:c.125A>G XP_011523671.1:p.Gln42Arg
XM_011525370.1:c.125A>G XP_011523672.1:p.Gln42Arg
XM_011525368.2:c.125A>G XP_011523670.1:p.Gln42Arg
XM_011525369.2:c.125A>G XP_011523671.1:p.Gln42Arg
XM_011525370.2:c.125A>G XP_011523672.1:p.Gln42Arg
XM_017025228.1:c.761A>G XP_016880717.1:p.Gln254Arg
XM_017025229.1:c.764A>G XP_016880718.1:p.Gln255Arg
XM_017025230.1:c.764A>G XP_016880719.1:p.Gln255Arg
XM_017025231.1:c.764A>G XP_016880720.1:p.Gln255Arg
NM_001369369.1:c.761A>G MANE Select NP_001356298.1:p.Gln254Arg
NM_003593.3:c.761A>G NP_003584.2:p.Gln254Arg