Canonical Allele Identifier: CA499088100
Gene: FOXN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26856153C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28529135C>G , CM000679.2:g.28529135C>G GRCh38
NC_000017.10:g.26856153C>G , CM000679.1:g.26856153C>G GRCh37
NC_000017.9:g.23880280C>G NCBI36
NG_007260.1:g.10195C>G , LRG_61:g.10195C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000577936.2:c.741C>G ENSP00000462159.2:p.Gly247=
ENST00000579795.6:c.741C>G MANE Select ENSP00000464645.1:p.Gly247=
ENST00000226247.2:c.741C>G ENSP00000226247.2:p.Gly247=
ENST00000481916.6:c.*1196-73026G>C ENSP00000436369.2:n.*1196-73026G>C
ENST00000579795.5:c.741C>G ENSP00000464645.1:p.Gly247=
NM_003593.2:c.741C>G , LRG_61t1:c.741C>G NP_003584.2:p.Gly247=
XM_005258046.3:c.741C>G XP_005258103.1:p.Gly247=
XM_011525354.1:c.798C>G XP_011523656.1:p.Gly266=
XM_011525355.1:c.795C>G XP_011523657.1:p.Gly265=
XM_011525356.1:c.795C>G XP_011523658.1:p.Gly265=
XM_011525357.1:c.777C>G XP_011523659.1:p.Gly259=
XM_011525358.1:c.744C>G XP_011523660.1:p.Gly248=
XM_011525359.1:c.744C>G XP_011523661.1:p.Gly248=
XM_011525360.1:c.744C>G XP_011523662.1:p.Gly248=
XM_011525361.1:c.741C>G XP_011523663.1:p.Gly247=
XM_011525362.1:c.741C>G XP_011523664.1:p.Gly247=
XM_011525363.1:c.798C>G XP_011523665.1:p.Gly266=
XM_011525364.1:c.276C>G XP_011523666.1:p.Gly92=
XM_011525365.1:c.798C>G XP_011523667.1:p.Gly266=
XM_011525366.1:c.198C>G XP_011523668.1:p.Gly66=
XM_011525367.1:c.183C>G XP_011523669.1:p.Gly61=
XM_011525368.1:c.105C>G XP_011523670.1:p.Gly35=
XM_011525369.1:c.105C>G XP_011523671.1:p.Gly35=
XM_011525370.1:c.105C>G XP_011523672.1:p.Gly35=
XM_011525368.2:c.105C>G XP_011523670.1:p.Gly35=
XM_011525369.2:c.105C>G XP_011523671.1:p.Gly35=
XM_011525370.2:c.105C>G XP_011523672.1:p.Gly35=
XM_017025228.1:c.741C>G XP_016880717.1:p.Gly247=
XM_017025229.1:c.744C>G XP_016880718.1:p.Gly248=
XM_017025230.1:c.744C>G XP_016880719.1:p.Gly248=
XM_017025231.1:c.744C>G XP_016880720.1:p.Gly248=
NM_001369369.1:c.741C>G MANE Select NP_001356298.1:p.Gly247=
NM_003593.3:c.741C>G NP_003584.2:p.Gly247=