Canonical Allele Identifier: CA2479950094
Gene: FLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152309110_152309114delinsCCTGA , CM000663.2:g.152309110_152309114delinsCCTGA GRCh38
NC_000001.10:g.152281586_152281590delinsCCTGA , CM000663.1:g.152281586_152281590delinsCCTGA GRCh37
NC_000001.9:g.150548210_150548214delinsCCTGA NCBI36
NG_016190.1:g.21090_21094delinsTCAGG , LRG_1028:g.21090_21094delinsTCAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5772_5776delinsTCAGG MANE Select ENSP00000357789.1:p.Ser1924=
ENST00000368799.1:c.5772_5776delinsTCAGG ENSP00000357789.1:p.Ser1924=
NM_002016.1:c.5772_5776delinsTCAGG , LRG_1028t1:c.5772_5776delinsTCAGG NP_002007.1:p.Ser1924=
XM_011509329.1:c.5772_5776delinsTCAGG XP_011507631.1:p.Ser1924=
NM_002016.2:c.5772_5776delinsTCAGG MANE Select NP_002007.1:p.Ser1924=
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