Canonical Allele Identifier: CA1142883741
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152309156T= , CM000663.2:g.152309156T= GRCh38
NC_000001.10:g.152281632T= , CM000663.1:g.152281632T= GRCh37
NC_000001.9:g.150548256T= NCBI36
NG_016190.1:g.21048A= , LRG_1028:g.21048A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5730A= MANE Select ENSP00000357789.1:p.Thr1910=
ENST00000368799.1:c.5730A= ENSP00000357789.1:p.Thr1910=
NM_002016.1:c.5730A= , LRG_1028t1:c.5730A= NP_002007.1:p.Thr1910=
XM_011509329.1:c.5730A= XP_011507631.1:p.Thr1910=
NM_002016.2:c.5730A= MANE Select NP_002007.1:p.Thr1910=