Canonical Allele Identifier: CA499418045

Gene: FOXN1

Linked Data

• MyVariant Identifiers: chr17:g.26861795T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28534777T>G , CM000679.2:g.28534777T>G	GRCh38
NC_000017.10:g.26861795T>G , CM000679.1:g.26861795T>G	GRCh37
NC_000017.9:g.23885922T>G	NCBI36
NG_007260.1:g.15837T>G , LRG_61:g.15837T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000577936.2:c.1206T>G	ENSP00000462159.2:p.Pro402=
ENST00000579795.6:c.1206T>G MANE Select	ENSP00000464645.1:p.Pro402=
ENST00000226247.2:c.1206T>G	ENSP00000226247.2:p.Pro402=
ENST00000481916.6:c.*1195+69274A>C	ENSP00000436369.2:n.*1195+69274A>C
ENST00000579795.5:c.1206T>G	ENSP00000464645.1:p.Pro402=
NM_003593.2:c.1206T>G , LRG_61t1:c.1206T>G	NP_003584.2:p.Pro402=
XM_005258046.3:c.1206T>G	XP_005258103.1:p.Pro402=
XM_011525354.1:c.1263T>G	XP_011523656.1:p.Pro421=
XM_011525355.1:c.1260T>G	XP_011523657.1:p.Pro420=
XM_011525356.1:c.1260T>G	XP_011523658.1:p.Pro420=
XM_011525357.1:c.1242T>G	XP_011523659.1:p.Pro414=
XM_011525358.1:c.1209T>G	XP_011523660.1:p.Pro403=
XM_011525359.1:c.1209T>G	XP_011523661.1:p.Pro403=
XM_011525360.1:c.1209T>G	XP_011523662.1:p.Pro403=
XM_011525361.1:c.1206T>G	XP_011523663.1:p.Pro402=
XM_011525362.1:c.1206T>G	XP_011523664.1:p.Pro402=
XM_011525363.1:c.1193-176T>G	XP_011523665.1:n.1193-176T>G
XM_011525364.1:c.741T>G	XP_011523666.1:p.Pro247=
XM_011525365.1:c.1192+239T>G	XP_011523667.1:n.1192+239T>G
XM_011525366.1:c.663T>G	XP_011523668.1:p.Pro221=
XM_011525367.1:c.648T>G	XP_011523669.1:p.Pro216=
XM_011525368.1:c.570T>G	XP_011523670.1:p.Pro190=
XM_011525369.1:c.570T>G	XP_011523671.1:p.Pro190=
XM_011525370.1:c.570T>G	XP_011523672.1:p.Pro190=
XM_011525368.2:c.570T>G	XP_011523670.1:p.Pro190=
XM_011525369.2:c.570T>G	XP_011523671.1:p.Pro190=
XM_011525370.2:c.570T>G	XP_011523672.1:p.Pro190=
XM_017025228.1:c.1206T>G	XP_016880717.1:p.Pro402=
XM_017025229.1:c.1139-176T>G	XP_016880718.1:n.1139-176T>G
XM_017025230.1:c.1138+239T>G	XP_016880719.1:n.1138+239T>G
XM_017025231.1:c.1139-217T>G	XP_016880720.1:n.1139-217T>G
NM_001369369.1:c.1206T>G MANE Select	NP_001356298.1:p.Pro402=
NM_003593.3:c.1206T>G	NP_003584.2:p.Pro402=