Canonical Allele Identifier: CA2479947766
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152305000A= , CM000663.2:g.152305000A= GRCh38
NC_000001.10:g.152277476A= , CM000663.1:g.152277476A= GRCh37
NC_000001.9:g.150544100A= NCBI36
NG_016190.1:g.25204T= , LRG_1028:g.25204T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9886T= MANE Select ENSP00000357789.1:p.Ser3296=
ENST00000368799.1:c.9886T= ENSP00000357789.1:p.Ser3296=
NM_002016.1:c.9886T= , LRG_1028t1:c.9886T= NP_002007.1:p.Ser3296=
XM_011509329.1:c.9108+778T= XP_011507631.1:n.9108+778T=
NM_002016.2:c.9886T= MANE Select NP_002007.1:p.Ser3296=