Canonical Allele Identifier: CA2647993568

Gene: FLG

Linked Data

• gnomAD v4: 1-152305030-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152305030_152305031insC , CM000663.2:g.152305030_152305031insC	GRCh38
NC_000001.10:g.152277506_152277507insC , CM000663.1:g.152277506_152277507insC	GRCh37
NC_000001.9:g.150544130_150544131insC	NCBI36
NG_016190.1:g.25173_25174insG , LRG_1028:g.25173_25174insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.9855_9856insG MANE Select	ENSP00000357789.1:p.Gln3286AlafsTer7
ENST00000368799.1:c.9855_9856insG	ENSP00000357789.1:p.Gln3286AlafsTer7
NM_002016.1:c.9855_9856insG , LRG_1028t1:c.9855_9856insG	NP_002007.1:p.Gln3286AlafsTer7
XM_011509329.1:c.9108+747_9108+748insG	XP_011507631.1:n.9108+747_9108+748insG
NM_002016.2:c.9855_9856insG MANE Select	NP_002007.1:p.Gln3286AlafsTer7