Canonical Allele Identifier: CA2479951889
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312381T= , CM000663.2:g.152312381T= GRCh38
NC_000001.10:g.152284857T= , CM000663.1:g.152284857T= GRCh37
NC_000001.9:g.150551481T= NCBI36
NG_016190.1:g.17823A= , LRG_1028:g.17823A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2505A= MANE Select ENSP00000357789.1:p.Gln835=
ENST00000368799.1:c.2505A= ENSP00000357789.1:p.Gln835=
NM_002016.1:c.2505A= , LRG_1028t1:c.2505A= NP_002007.1:p.Gln835=
XM_011509329.1:c.2505A= XP_011507631.1:p.Gln835=
NM_002016.2:c.2505A= MANE Select NP_002007.1:p.Gln835=