Canonical Allele Identifier: CA1141894834
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304963T= , CM000663.2:g.152304963T= GRCh38
NC_000001.10:g.152277439T= , CM000663.1:g.152277439T= GRCh37
NC_000001.9:g.150544063T= NCBI36
NG_016190.1:g.25241A= , LRG_1028:g.25241A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9923A= MANE Select ENSP00000357789.1:p.Gln3308=
ENST00000368799.1:c.9923A= ENSP00000357789.1:p.Gln3308=
NM_002016.1:c.9923A= , LRG_1028t1:c.9923A= NP_002007.1:p.Gln3308=
XM_011509329.1:c.9108+815A= XP_011507631.1:n.9108+815A=
NM_002016.2:c.9923A= MANE Select NP_002007.1:p.Gln3308=