Canonical Allele Identifier: CA1148409394
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152310449G= , CM000663.2:g.152310449G= GRCh38
NC_000001.10:g.152282925G= , CM000663.1:g.152282925G= GRCh37
NC_000001.9:g.150549549G= NCBI36
NG_016190.1:g.19755C= , LRG_1028:g.19755C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.4437C= MANE Select ENSP00000357789.1:p.His1479=
ENST00000368799.1:c.4437C= ENSP00000357789.1:p.His1479=
NM_002016.1:c.4437C= , LRG_1028t1:c.4437C= NP_002007.1:p.His1479=
XM_011509329.1:c.4437C= XP_011507631.1:p.His1479=
NM_002016.2:c.4437C= MANE Select NP_002007.1:p.His1479=