Canonical Allele Identifier: CA2647993758

Gene: FLG

Linked Data

• gnomAD v4: 1-152312444-AGTGCTGGGCCCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152312447_152312458del , CM000663.2:g.152312447_152312458del	GRCh38
NC_000001.10:g.152284923_152284934del , CM000663.1:g.152284923_152284934del	GRCh37
NC_000001.9:g.150551547_150551558del	NCBI36
NG_016190.1:g.17748_17759del , LRG_1028:g.17748_17759del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.2430_2441del MANE Select	ENSP00000357789.1:p.Gly811_Thr814del
ENST00000368799.1:c.2430_2441del	ENSP00000357789.1:p.Gly811_Thr814del
NM_002016.1:c.2430_2441del , LRG_1028t1:c.2430_2441del	NP_002007.1:p.Gly811_Thr814del
XM_011509329.1:c.2430_2441del	XP_011507631.1:p.Gly811_Thr814del
NM_002016.2:c.2430_2441del MANE Select	NP_002007.1:p.Gly811_Thr814del