Canonical Allele Identifier: CA2479950863
Gene: FLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152310436_152310444delinsCTTGGGATG , CM000663.2:g.152310436_152310444delinsCTTGGGATG GRCh38
NC_000001.10:g.152282912_152282920delinsCTTGGGATG , CM000663.1:g.152282912_152282920delinsCTTGGGATG GRCh37
NC_000001.9:g.150549536_150549544delinsCTTGGGATG NCBI36
NG_016190.1:g.19760_19768delinsCATCCCAAG , LRG_1028:g.19760_19768delinsCATCCCAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.4442_4450delinsCATCCCAAG MANE Select ENSP00000357789.1:p.Ala1481=
ENST00000368799.1:c.4442_4450delinsCATCCCAAG ENSP00000357789.1:p.Ala1481=
NM_002016.1:c.4442_4450delinsCATCCCAAG , LRG_1028t1:c.4442_4450delinsCATCCCAAG NP_002007.1:p.Ala1481=
XM_011509329.1:c.4442_4450delinsCATCCCAAG XP_011507631.1:p.Ala1481=
NM_002016.2:c.4442_4450delinsCATCCCAAG MANE Select NP_002007.1:p.Ala1481=
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