Canonical Allele Identifier: CA8459381

Gene: FOXN1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28530770T>C , CM000679.2:g.28530770T>C	GRCh38
NC_000017.10:g.26857788T>C , CM000679.1:g.26857788T>C	GRCh37
NC_000017.9:g.23881915T>C	NCBI36
NG_007260.1:g.11830T>C , LRG_61:g.11830T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577936.2:c.852T>C	ENSP00000462159.2:p.Leu284=
ENST00000579795.6:c.852T>C MANE Select	ENSP00000464645.1:p.Leu284=
ENST00000226247.2:c.852T>C	ENSP00000226247.2:p.Leu284=
ENST00000481916.6:c.*1195+73281A>G	ENSP00000436369.2:n.*1195+73281A>G
ENST00000579795.5:c.852T>C	ENSP00000464645.1:p.Leu284=
NM_003593.2:c.852T>C , LRG_61t1:c.852T>C	NP_003584.2:p.Leu284=
XM_005258046.3:c.852T>C	XP_005258103.1:p.Leu284=
XM_011525354.1:c.909T>C	XP_011523656.1:p.Leu303=
XM_011525355.1:c.906T>C	XP_011523657.1:p.Leu302=
XM_011525356.1:c.906T>C	XP_011523658.1:p.Leu302=
XM_011525357.1:c.888T>C	XP_011523659.1:p.Leu296=
XM_011525358.1:c.855T>C	XP_011523660.1:p.Leu285=
XM_011525359.1:c.855T>C	XP_011523661.1:p.Leu285=
XM_011525360.1:c.855T>C	XP_011523662.1:p.Leu285=
XM_011525361.1:c.852T>C	XP_011523663.1:p.Leu284=
XM_011525362.1:c.852T>C	XP_011523664.1:p.Leu284=
XM_011525363.1:c.909T>C	XP_011523665.1:p.Leu303=
XM_011525364.1:c.387T>C	XP_011523666.1:p.Leu129=
XM_011525365.1:c.909T>C	XP_011523667.1:p.Leu303=
XM_011525366.1:c.309T>C	XP_011523668.1:p.Leu103=
XM_011525367.1:c.294T>C	XP_011523669.1:p.Leu98=
XM_011525368.1:c.216T>C	XP_011523670.1:p.Leu72=
XM_011525369.1:c.216T>C	XP_011523671.1:p.Leu72=
XM_011525370.1:c.216T>C	XP_011523672.1:p.Leu72=
XM_011525368.2:c.216T>C	XP_011523670.1:p.Leu72=
XM_011525369.2:c.216T>C	XP_011523671.1:p.Leu72=
XM_011525370.2:c.216T>C	XP_011523672.1:p.Leu72=
XM_017025228.1:c.852T>C	XP_016880717.1:p.Leu284=
XM_017025229.1:c.855T>C	XP_016880718.1:p.Leu285=
XM_017025230.1:c.855T>C	XP_016880719.1:p.Leu285=
XM_017025231.1:c.855T>C	XP_016880720.1:p.Leu285=
NM_001369369.1:c.852T>C MANE Select	NP_001356298.1:p.Leu284=
NM_003593.3:c.852T>C	NP_003584.2:p.Leu284=