Canonical Allele Identifier: CA2254348258

Gene: FOXN1

Linked Data

• ClinVar Variation Id: 3016233
• ClinVar RCV Id: RCV003876384
• dbSNP Id: rs2070008472

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28534691C>G , CM000679.2:g.28534691C>G	GRCh38
NC_000017.10:g.26861709C>G , CM000679.1:g.26861709C>G	GRCh37
NC_000017.9:g.23885836C>G	NCBI36
NG_007260.1:g.15751C>G , LRG_61:g.15751C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000577936.2:c.1136-16C>G	ENSP00000462159.2:n.1136-16C>G
ENST00000579795.6:c.1136-16C>G MANE Select	ENSP00000464645.1:n.1136-16C>G
ENST00000226247.2:c.1136-16C>G	ENSP00000226247.2:n.1136-16C>G
ENST00000481916.6:c.*1195+69360G>C	ENSP00000436369.2:n.*1195+69360G>C
ENST00000579795.5:c.1136-16C>G	ENSP00000464645.1:n.1136-16C>G
NM_003593.2:c.1136-16C>G , LRG_61t1:c.1136-16C>G	NP_003584.2:n.1136-16C>G
XM_005258046.3:c.1136-16C>G	XP_005258103.1:n.1136-16C>G
XM_011525354.1:c.1193-16C>G	XP_011523656.1:n.1193-16C>G
XM_011525355.1:c.1190-16C>G	XP_011523657.1:n.1190-16C>G
XM_011525356.1:c.1190-16C>G	XP_011523658.1:n.1190-16C>G
XM_011525357.1:c.1172-16C>G	XP_011523659.1:n.1172-16C>G
XM_011525358.1:c.1139-16C>G	XP_011523660.1:n.1139-16C>G
XM_011525359.1:c.1139-16C>G	XP_011523661.1:n.1139-16C>G
XM_011525360.1:c.1139-16C>G	XP_011523662.1:n.1139-16C>G
XM_011525361.1:c.1136-16C>G	XP_011523663.1:n.1136-16C>G
XM_011525362.1:c.1136-16C>G	XP_011523664.1:n.1136-16C>G
XM_011525363.1:c.1192+153C>G	XP_011523665.1:n.1192+153C>G
XM_011525364.1:c.671-16C>G	XP_011523666.1:n.671-16C>G
XM_011525365.1:c.1192+153C>G	XP_011523667.1:n.1192+153C>G
XM_011525366.1:c.593-16C>G	XP_011523668.1:n.593-16C>G
XM_011525367.1:c.578-16C>G	XP_011523669.1:n.578-16C>G
XM_011525368.1:c.500-16C>G	XP_011523670.1:n.500-16C>G
XM_011525369.1:c.500-16C>G	XP_011523671.1:n.500-16C>G
XM_011525370.1:c.500-16C>G	XP_011523672.1:n.500-16C>G
XM_011525368.2:c.500-16C>G	XP_011523670.1:n.500-16C>G
XM_011525369.2:c.500-16C>G	XP_011523671.1:n.500-16C>G
XM_011525370.2:c.500-16C>G	XP_011523672.1:n.500-16C>G
XM_017025228.1:c.1136-16C>G	XP_016880717.1:n.1136-16C>G
XM_017025229.1:c.1138+153C>G	XP_016880718.1:n.1138+153C>G
XM_017025230.1:c.1138+153C>G	XP_016880719.1:n.1138+153C>G
XM_017025231.1:c.1138+153C>G	XP_016880720.1:n.1138+153C>G
NM_001369369.1:c.1136-16C>G MANE Select	NP_001356298.1:n.1136-16C>G
NM_003593.3:c.1136-16C>G	NP_003584.2:n.1136-16C>G