Canonical Allele Identifier: CA499086139

Gene: FOXN1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28523999C>T , CM000679.2:g.28523999C>T	GRCh38
NC_000017.10:g.26851017C>T , CM000679.1:g.26851017C>T	GRCh37
NC_000017.9:g.23875144C>T	NCBI36
NG_007260.1:g.5059C>T , LRG_61:g.5059C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001369369.1:c.30C>T MANE Select	NP_001356298.1:p.Asp10=
ENST00000579795.6:c.30C>T MANE Select	ENSP00000464645.1:p.Asp10=
NM_003593.2:c.30C>T , LRG_61t1:c.30C>T	NP_003584.2:p.Asp10=
NM_003593.3:c.30C>T	NP_003584.2:p.Asp10=
ENST00000226247.2:c.30C>T	ENSP00000226247.2:p.Asp10=
ENST00000481916.6:c.*1196-67890G>A	ENSP00000436369.2:n.*1196-67890G>A
ENST00000577936.1:c.30C>T	ENSP00000462159.1:p.Asp10=
ENST00000577936.2:c.30C>T	ENSP00000462159.2:p.Asp10=
ENST00000579795.5:c.30C>T	ENSP00000464645.1:p.Asp10=
XM_005258046.3:c.30C>T	XP_005258103.1:p.Asp10=
XM_011525354.1:c.84C>T	XP_011523656.1:p.Asp28=
XM_011525355.1:c.84C>T	XP_011523657.1:p.Asp28=
XM_011525356.1:c.84C>T	XP_011523658.1:p.Asp28=
XM_011525357.1:c.63C>T	XP_011523659.1:p.Asp21=
XM_011525358.1:c.30C>T	XP_011523660.1:p.Asp10=
XM_011525359.1:c.30C>T	XP_011523661.1:p.Asp10=
XM_011525360.1:c.30C>T	XP_011523662.1:p.Asp10=
XM_011525361.1:c.30C>T	XP_011523663.1:p.Asp10=
XM_011525362.1:c.30C>T	XP_011523664.1:p.Asp10=
XM_011525363.1:c.84C>T	XP_011523665.1:p.Asp28=
XM_011525364.1:c.30C>T	XP_011523666.1:p.Asp10=
XM_011525365.1:c.84C>T	XP_011523667.1:p.Asp28=
XM_011525366.1:c.46-3252C>T	XP_011523668.1:n.46-3252C>T
XM_011525368.1:c.-51-3249C>T	XP_011523670.1:n.-51-3249C>T
XM_011525368.2:c.-51-3249C>T	XP_011523670.1:n.-51-3249C>T
XM_017025228.1:c.30C>T	XP_016880717.1:p.Asp10=
XM_017025229.1:c.30C>T	XP_016880718.1:p.Asp10=
XM_017025230.1:c.30C>T	XP_016880719.1:p.Asp10=
XM_017025231.1:c.30C>T	XP_016880720.1:p.Asp10=