Canonical Allele Identifier: CA1148466990
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152310956_152310958delinsCCC , CM000663.2:g.152310956_152310958delinsCCC GRCh38
NC_000001.10:g.152283432_152283434delinsCCC , CM000663.1:g.152283432_152283434delinsCCC GRCh37
NC_000001.9:g.150550056_150550058delinsCCC NCBI36
NG_016190.1:g.19246_19248delinsGGG , LRG_1028:g.19246_19248delinsGGG

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.3928_3930delinsGGG MANE Select ENSP00000357789.1:p.Gly1310=
ENST00000368799.1:c.3928_3930delinsGGG ENSP00000357789.1:p.Gly1310=
NM_002016.1:c.3928_3930delinsGGG , LRG_1028t1:c.3928_3930delinsGGG NP_002007.1:p.Gly1310=
XM_011509329.1:c.3928_3930delinsGGG XP_011507631.1:p.Gly1310=
NM_002016.2:c.3928_3930delinsGGG MANE Select NP_002007.1:p.Gly1310=