Canonical Allele Identifier: CA2479949249
Gene: FLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152307649_152307658delinsACCCTGAACG , CM000663.2:g.152307649_152307658delinsACCCTGAACG GRCh38
NC_000001.10:g.152280125_152280134delinsACCCTGAACG , CM000663.1:g.152280125_152280134delinsACCCTGAACG GRCh37
NC_000001.9:g.150546749_150546758delinsACCCTGAACG NCBI36
NG_016190.1:g.22546_22555delinsCGTTCAGGGT , LRG_1028:g.22546_22555delinsCGTTCAGGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.7228_7237delinsCGTTCAGGGT MANE Select ENSP00000357789.1:p.Arg2410=
ENST00000368799.1:c.7228_7237delinsCGTTCAGGGT ENSP00000357789.1:p.Arg2410=
NM_002016.1:c.7228_7237delinsCGTTCAGGGT , LRG_1028t1:c.7228_7237delinsCGTTCAGGGT NP_002007.1:p.Arg2410=
XM_011509329.1:c.7228_7237delinsCGTTCAGGGT XP_011507631.1:p.Arg2410=
NM_002016.2:c.7228_7237delinsCGTTCAGGGT MANE Select NP_002007.1:p.Arg2410=
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