Canonical Allele Identifier: CA2479947563
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304665A= , CM000663.2:g.152304665A= GRCh38
NC_000001.10:g.152277141A= , CM000663.1:g.152277141A= GRCh37
NC_000001.9:g.150543765A= NCBI36
NG_016190.1:g.25539T= , LRG_1028:g.25539T=

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.10221T= MANE Select ENSP00000357789.1:p.Thr3407=
ENST00000368799.1:c.10221T= ENSP00000357789.1:p.Thr3407=
NM_002016.1:c.10221T= , LRG_1028t1:c.10221T= NP_002007.1:p.Thr3407=
XM_011509329.1:c.9109-832T= XP_011507631.1:n.9109-832T=
NM_002016.2:c.10221T= MANE Select NP_002007.1:p.Thr3407=