Canonical Allele Identifier: CA2746127707
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311222_152311223insGTC , CM000663.2:g.152311222_152311223insGTC GRCh38
NC_000001.10:g.152283698_152283699insGTC , CM000663.1:g.152283698_152283699insGTC GRCh37
NC_000001.9:g.150550322_150550323insGTC NCBI36
NG_016190.1:g.18981_18982insGAC , LRG_1028:g.18981_18982insGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.3663_3664insGAC MANE Select ENSP00000357789.1:p.Arg1221_Lys1222insAsp
ENST00000368799.1:c.3663_3664insGAC ENSP00000357789.1:p.Arg1221_Lys1222insAsp
NM_002016.1:c.3663_3664insGAC , LRG_1028t1:c.3663_3664insGAC NP_002007.1:p.Arg1221_Lys1222insAsp
XM_011509329.1:c.3663_3664insGAC XP_011507631.1:p.Arg1221_Lys1222insAsp
NM_002016.2:c.3663_3664insGAC MANE Select NP_002007.1:p.Arg1221_Lys1222insAsp