Canonical Allele Identifier: CA2479947677
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304848A= , CM000663.2:g.152304848A= GRCh38
NC_000001.10:g.152277324A= , CM000663.1:g.152277324A= GRCh37
NC_000001.9:g.150543948A= NCBI36
NG_016190.1:g.25356T= , LRG_1028:g.25356T=

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.10038T= MANE Select ENSP00000357789.1:p.His3346=
ENST00000368799.1:c.10038T= ENSP00000357789.1:p.His3346=
NM_002016.1:c.10038T= , LRG_1028t1:c.10038T= NP_002007.1:p.His3346=
XM_011509329.1:c.9108+930T= XP_011507631.1:n.9108+930T=
NM_002016.2:c.10038T= MANE Select NP_002007.1:p.His3346=