Canonical Allele Identifier: CA1146841011
Gene: FLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152309149T= , CM000663.2:g.152309149T= GRCh38
NC_000001.10:g.152281625T= , CM000663.1:g.152281625T= GRCh37
NC_000001.9:g.150548249T= NCBI36
NG_016190.1:g.21055A= , LRG_1028:g.21055A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5737A= MANE Select ENSP00000357789.1:p.Asn1913=
ENST00000368799.1:c.5737A= ENSP00000357789.1:p.Asn1913=
NM_002016.1:c.5737A= , LRG_1028t1:c.5737A= NP_002007.1:p.Asn1913=
XM_011509329.1:c.5737A= XP_011507631.1:p.Asn1913=
NM_002016.2:c.5737A= MANE Select NP_002007.1:p.Asn1913=
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