Canonical Allele Identifier: CA2647993604
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152310913_152310972dup , CM000663.2:g.152310913_152310972dup GRCh38
NC_000001.10:g.152283389_152283448dup , CM000663.1:g.152283389_152283448dup GRCh37
NC_000001.9:g.150550013_150550072dup NCBI36
NG_016190.1:g.19242_19301dup , LRG_1028:g.19242_19301dup

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.3924_3983dup MANE Select ENSP00000357789.1:p.Arg1327_Gln1328insHis...
ENST00000368799.1:c.3924_3983dup ENSP00000357789.1:p.Arg1327_Gln1328insHis...
NM_002016.1:c.3924_3983dup , LRG_1028t1:c.3924_3983dup NP_002007.1:p.Arg1327_Gln1328insHisProGly...
XM_011509329.1:c.3924_3983dup XP_011507631.1:p.Arg1327_Gln1328insHisPro...
NM_002016.2:c.3924_3983dup MANE Select NP_002007.1:p.Arg1327_Gln1328insHisProGly...