Canonical Allele Identifier: CA2254345678

Gene: FOXN1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28529122T= , CM000679.2:g.28529122T=	GRCh38
NC_000017.10:g.26856140T= , CM000679.1:g.26856140T=	GRCh37
NC_000017.9:g.23880267T=	NCBI36
NG_007260.1:g.10182T= , LRG_61:g.10182T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577936.2:c.728T=	ENSP00000462159.2:p.Ile243=
ENST00000579795.6:c.728T= MANE Select	ENSP00000464645.1:p.Ile243=
ENST00000226247.2:c.728T=	ENSP00000226247.2:p.Ile243=
ENST00000481916.6:c.*1196-73013A=	ENSP00000436369.2:n.*1196-73013A=
ENST00000579795.5:c.728T=	ENSP00000464645.1:p.Ile243=
NM_003593.2:c.728T= , LRG_61t1:c.728T=	NP_003584.2:p.Ile243=
XM_005258046.3:c.728T=	XP_005258103.1:p.Ile243=
XM_011525354.1:c.785T=	XP_011523656.1:p.Ile262=
XM_011525355.1:c.782T=	XP_011523657.1:p.Ile261=
XM_011525356.1:c.782T=	XP_011523658.1:p.Ile261=
XM_011525357.1:c.764T=	XP_011523659.1:p.Ile255=
XM_011525358.1:c.731T=	XP_011523660.1:p.Ile244=
XM_011525359.1:c.731T=	XP_011523661.1:p.Ile244=
XM_011525360.1:c.731T=	XP_011523662.1:p.Ile244=
XM_011525361.1:c.728T=	XP_011523663.1:p.Ile243=
XM_011525362.1:c.728T=	XP_011523664.1:p.Ile243=
XM_011525363.1:c.785T=	XP_011523665.1:p.Ile262=
XM_011525364.1:c.263T=	XP_011523666.1:p.Ile88=
XM_011525365.1:c.785T=	XP_011523667.1:p.Ile262=
XM_011525366.1:c.185T=	XP_011523668.1:p.Ile62=
XM_011525367.1:c.170T=	XP_011523669.1:p.Ile57=
XM_011525368.1:c.92T=	XP_011523670.1:p.Ile31=
XM_011525369.1:c.92T=	XP_011523671.1:p.Ile31=
XM_011525370.1:c.92T=	XP_011523672.1:p.Ile31=
XM_011525368.2:c.92T=	XP_011523670.1:p.Ile31=
XM_011525369.2:c.92T=	XP_011523671.1:p.Ile31=
XM_011525370.2:c.92T=	XP_011523672.1:p.Ile31=
XM_017025228.1:c.728T=	XP_016880717.1:p.Ile243=
XM_017025229.1:c.731T=	XP_016880718.1:p.Ile244=
XM_017025230.1:c.731T=	XP_016880719.1:p.Ile244=
XM_017025231.1:c.731T=	XP_016880720.1:p.Ile244=
NM_001369369.1:c.728T= MANE Select	NP_001356298.1:p.Ile243=
NM_003593.3:c.728T=	NP_003584.2:p.Ile243=