Canonical Allele Identifier: CA2479951987
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312568T= , CM000663.2:g.152312568T= GRCh38
NC_000001.10:g.152285044T= , CM000663.1:g.152285044T= GRCh37
NC_000001.9:g.150551668T= NCBI36
NG_016190.1:g.17636A= , LRG_1028:g.17636A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2318A= MANE Select ENSP00000357789.1:p.Gln773=
ENST00000368799.1:c.2318A= ENSP00000357789.1:p.Gln773=
NM_002016.1:c.2318A= , LRG_1028t1:c.2318A= NP_002007.1:p.Gln773=
XM_011509329.1:c.2318A= XP_011507631.1:p.Gln773=
NM_002016.2:c.2318A= MANE Select NP_002007.1:p.Gln773=