Canonical Allele Identifier: CA2647993468

Gene: FLG

Linked Data

• gnomAD v4: 1-152304237-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304238del , CM000663.2:g.152304238del	GRCh38
NC_000001.10:g.152276714del , CM000663.1:g.152276714del	GRCh37
NC_000001.9:g.150543338del	NCBI36
NG_016190.1:g.25966del , LRG_1028:g.25966del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.10648del MANE Select	ENSP00000357789.1:p.Glu3550LysfsTer?
ENST00000368799.1:c.10648del	ENSP00000357789.1:p.Glu3550LysfsTer?
NM_002016.1:c.10648del , LRG_1028t1:c.10648del	NP_002007.1:p.Glu3550LysfsTer?
XM_011509329.1:c.9109-405del	XP_011507631.1:n.9109-405del
NM_002016.2:c.10648del MANE Select	NP_002007.1:p.Glu3550LysfsTer?