Canonical Allele Identifier: CA398323136

Gene: FOXN1

Linked Data

• MyVariant Identifiers: chr17:g.26856174G>C (hg19) ; chr17:g.28529156G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28529156G>C , CM000679.2:g.28529156G>C	GRCh38
NC_000017.10:g.26856174G>C , CM000679.1:g.26856174G>C	GRCh37
NC_000017.9:g.23880301G>C	NCBI36
NG_007260.1:g.10216G>C , LRG_61:g.10216G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577936.2:c.762G>C	ENSP00000462159.2:p.Gln254His
ENST00000579795.6:c.762G>C MANE Select	ENSP00000464645.1:p.Gln254His
ENST00000226247.2:c.762G>C	ENSP00000226247.2:p.Gln254His
ENST00000481916.6:c.*1196-73047C>G	ENSP00000436369.2:n.*1196-73047C>G
ENST00000579795.5:c.762G>C	ENSP00000464645.1:p.Gln254His
NM_003593.2:c.762G>C , LRG_61t1:c.762G>C	NP_003584.2:p.Gln254His
XM_005258046.3:c.762G>C	XP_005258103.1:p.Gln254His
XM_011525354.1:c.819G>C	XP_011523656.1:p.Gln273His
XM_011525355.1:c.816G>C	XP_011523657.1:p.Gln272His
XM_011525356.1:c.816G>C	XP_011523658.1:p.Gln272His
XM_011525357.1:c.798G>C	XP_011523659.1:p.Gln266His
XM_011525358.1:c.765G>C	XP_011523660.1:p.Gln255His
XM_011525359.1:c.765G>C	XP_011523661.1:p.Gln255His
XM_011525360.1:c.765G>C	XP_011523662.1:p.Gln255His
XM_011525361.1:c.762G>C	XP_011523663.1:p.Gln254His
XM_011525362.1:c.762G>C	XP_011523664.1:p.Gln254His
XM_011525363.1:c.819G>C	XP_011523665.1:p.Gln273His
XM_011525364.1:c.297G>C	XP_011523666.1:p.Gln99His
XM_011525365.1:c.819G>C	XP_011523667.1:p.Gln273His
XM_011525366.1:c.219G>C	XP_011523668.1:p.Gln73His
XM_011525367.1:c.204G>C	XP_011523669.1:p.Gln68His
XM_011525368.1:c.126G>C	XP_011523670.1:p.Gln42His
XM_011525369.1:c.126G>C	XP_011523671.1:p.Gln42His
XM_011525370.1:c.126G>C	XP_011523672.1:p.Gln42His
XM_011525368.2:c.126G>C	XP_011523670.1:p.Gln42His
XM_011525369.2:c.126G>C	XP_011523671.1:p.Gln42His
XM_011525370.2:c.126G>C	XP_011523672.1:p.Gln42His
XM_017025228.1:c.762G>C	XP_016880717.1:p.Gln254His
XM_017025229.1:c.765G>C	XP_016880718.1:p.Gln255His
XM_017025230.1:c.765G>C	XP_016880719.1:p.Gln255His
XM_017025231.1:c.765G>C	XP_016880720.1:p.Gln255His
NM_001369369.1:c.762G>C MANE Select	NP_001356298.1:p.Gln254His
NM_003593.3:c.762G>C	NP_003584.2:p.Gln254His