Canonical Allele Identifier: CA2479953350
Gene: FLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152315279A= , CM000663.2:g.152315279A= GRCh38
NC_000001.10:g.152287755A= , CM000663.1:g.152287755A= GRCh37
NC_000001.9:g.150554379A= NCBI36
NG_016190.1:g.14925T= , LRG_1028:g.14925T=

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.138+40T= MANE Select ENSP00000357789.1:n.138+40T=
ENST00000368799.1:c.138+40T= ENSP00000357789.1:n.138+40T=
NM_002016.1:c.138+40T= , LRG_1028t1:c.138+40T= NP_002007.1:n.138+40T=
NR_103778.1:n.914+322A=
XM_011509329.1:c.138+40T= XP_011507631.1:n.138+40T=
NM_002016.2:c.138+40T= MANE Select NP_002007.1:n.138+40T=
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