Canonical Allele Identifier: CA398325512

Gene: FOXN1

Linked Data

• ClinVar Variation Id: 856387
• ClinVar RCV Id: RCV001061838
• dbSNP Id: rs1365407291
• gnomAD v3: 17-28534778-G-A
• gnomAD v4: 17-28534778-G-A
• MyVariant Identifiers: chr17:g.26861796G>A (hg19) ; chr17:g.28534778G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28534778G>A , CM000679.2:g.28534778G>A	GRCh38
NC_000017.10:g.26861796G>A , CM000679.1:g.26861796G>A	GRCh37
NC_000017.9:g.23885923G>A	NCBI36
NG_007260.1:g.15838G>A , LRG_61:g.15838G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000577936.2:c.1207G>A	ENSP00000462159.2:p.Gly403Arg
ENST00000579795.6:c.1207G>A MANE Select	ENSP00000464645.1:p.Gly403Arg
ENST00000226247.2:c.1207G>A	ENSP00000226247.2:p.Gly403Arg
ENST00000481916.6:c.*1195+69273C>T	ENSP00000436369.2:n.*1195+69273C>T
ENST00000579795.5:c.1207G>A	ENSP00000464645.1:p.Gly403Arg
NM_003593.2:c.1207G>A , LRG_61t1:c.1207G>A	NP_003584.2:p.Gly403Arg
XM_005258046.3:c.1207G>A	XP_005258103.1:p.Gly403Arg
XM_011525354.1:c.1264G>A	XP_011523656.1:p.Gly422Arg
XM_011525355.1:c.1261G>A	XP_011523657.1:p.Gly421Arg
XM_011525356.1:c.1261G>A	XP_011523658.1:p.Gly421Arg
XM_011525357.1:c.1243G>A	XP_011523659.1:p.Gly415Arg
XM_011525358.1:c.1210G>A	XP_011523660.1:p.Gly404Arg
XM_011525359.1:c.1210G>A	XP_011523661.1:p.Gly404Arg
XM_011525360.1:c.1210G>A	XP_011523662.1:p.Gly404Arg
XM_011525361.1:c.1207G>A	XP_011523663.1:p.Gly403Arg
XM_011525362.1:c.1207G>A	XP_011523664.1:p.Gly403Arg
XM_011525363.1:c.1193-175G>A	XP_011523665.1:n.1193-175G>A
XM_011525364.1:c.742G>A	XP_011523666.1:p.Gly248Arg
XM_011525365.1:c.1192+240G>A	XP_011523667.1:n.1192+240G>A
XM_011525366.1:c.664G>A	XP_011523668.1:p.Gly222Arg
XM_011525367.1:c.649G>A	XP_011523669.1:p.Gly217Arg
XM_011525368.1:c.571G>A	XP_011523670.1:p.Gly191Arg
XM_011525369.1:c.571G>A	XP_011523671.1:p.Gly191Arg
XM_011525370.1:c.571G>A	XP_011523672.1:p.Gly191Arg
XM_011525368.2:c.571G>A	XP_011523670.1:p.Gly191Arg
XM_011525369.2:c.571G>A	XP_011523671.1:p.Gly191Arg
XM_011525370.2:c.571G>A	XP_011523672.1:p.Gly191Arg
XM_017025228.1:c.1207G>A	XP_016880717.1:p.Gly403Arg
XM_017025229.1:c.1139-175G>A	XP_016880718.1:n.1139-175G>A
XM_017025230.1:c.1138+240G>A	XP_016880719.1:n.1138+240G>A
XM_017025231.1:c.1139-216G>A	XP_016880720.1:n.1139-216G>A
NM_001369369.1:c.1207G>A MANE Select	NP_001356298.1:p.Gly403Arg
NM_003593.3:c.1207G>A	NP_003584.2:p.Gly403Arg