Canonical Allele Identifier: CA2479951347
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311393_152311394delinsTG , CM000663.2:g.152311393_152311394delinsTG GRCh38
NC_000001.10:g.152283869_152283870delinsTG , CM000663.1:g.152283869_152283870delinsTG GRCh37
NC_000001.9:g.150550493_150550494delinsTG NCBI36
NG_016190.1:g.18810_18811delinsCA , LRG_1028:g.18810_18811delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.3492_3493delinsCA MANE Select ENSP00000357789.1:p.Thr1164=
ENST00000368799.1:c.3492_3493delinsCA ENSP00000357789.1:p.Thr1164=
NM_002016.1:c.3492_3493delinsCA , LRG_1028t1:c.3492_3493delinsCA NP_002007.1:p.Thr1164=
XM_011509329.1:c.3492_3493delinsCA XP_011507631.1:p.Thr1164=
NM_002016.2:c.3492_3493delinsCA MANE Select NP_002007.1:p.Thr1164=