Canonical Allele Identifier: CA398322535
Community Standard Title: NM_001369369.1(FOXN1):c.699+1G>T
Gene: FOXN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28527362G>T , CM000679.2:g.28527362G>T GRCh38
NC_000017.10:g.26854380G>T , CM000679.1:g.26854380G>T GRCh37
NC_000017.9:g.23878507G>T NCBI36
NG_007260.1:g.8422G>T , LRG_61:g.8422G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001369369.1:c.699+1G>T MANE Select NP_001356298.1:n.699+1G>T
ENST00000579795.6:c.699+1G>T MANE Select ENSP00000464645.1:n.699+1G>T
NM_003593.2:c.699+1G>T , LRG_61t1:c.699+1G>T NP_003584.2:n.699+1G>T
NM_003593.3:c.699+1G>T NP_003584.2:n.699+1G>T
ENST00000226247.2:c.699+1G>T ENSP00000226247.2:n.699+1G>T
ENST00000481916.6:c.*1196-71253C>A ENSP00000436369.2:n.*1196-71253C>A
ENST00000577936.2:c.699+1G>T ENSP00000462159.2:n.699+1G>T
ENST00000579795.5:c.699+1G>T ENSP00000464645.1:n.699+1G>T
XM_005258046.3:c.699+1G>T XP_005258103.1:n.699+1G>T
XM_011525354.1:c.756+1G>T XP_011523656.1:n.756+1G>T
XM_011525355.1:c.753+1G>T XP_011523657.1:n.753+1G>T
XM_011525356.1:c.753+1G>T XP_011523658.1:n.753+1G>T
XM_011525357.1:c.735+1G>T XP_011523659.1:n.735+1G>T
XM_011525358.1:c.702+1G>T XP_011523660.1:n.702+1G>T
XM_011525359.1:c.702+1G>T XP_011523661.1:n.702+1G>T
XM_011525360.1:c.702+1G>T XP_011523662.1:n.702+1G>T
XM_011525361.1:c.699+1G>T XP_011523663.1:n.699+1G>T
XM_011525362.1:c.699+1G>T XP_011523664.1:n.699+1G>T
XM_011525363.1:c.756+1G>T XP_011523665.1:n.756+1G>T
XM_011525364.1:c.234+1G>T XP_011523666.1:n.234+1G>T
XM_011525365.1:c.756+1G>T XP_011523667.1:n.756+1G>T
XM_011525366.1:c.156+1G>T XP_011523668.1:n.156+1G>T
XM_011525367.1:c.141+1G>T XP_011523669.1:n.141+1G>T
XM_011525368.1:c.63+1G>T XP_011523670.1:n.63+1G>T
XM_011525368.2:c.63+1G>T XP_011523670.1:n.63+1G>T
XM_011525369.1:c.63+1G>T XP_011523671.1:n.63+1G>T
XM_011525369.2:c.63+1G>T XP_011523671.1:n.63+1G>T
XM_011525370.1:c.63+1G>T XP_011523672.1:n.63+1G>T
XM_011525370.2:c.63+1G>T XP_011523672.1:n.63+1G>T
XM_017025228.1:c.699+1G>T XP_016880717.1:n.699+1G>T
XM_017025229.1:c.702+1G>T XP_016880718.1:n.702+1G>T
XM_017025230.1:c.702+1G>T XP_016880719.1:n.702+1G>T
XM_017025231.1:c.702+1G>T XP_016880720.1:n.702+1G>T