Canonical Allele Identifier: CA1007766391

Gene: FLG

Linked Data

• gnomAD v3: 1-152307701-GC-G
• gnomAD v4: 1-152307701-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152307702del , CM000663.2:g.152307702del	GRCh38
NC_000001.10:g.152280178del , CM000663.1:g.152280178del	GRCh37
NC_000001.9:g.150546802del	NCBI36
NG_016190.1:g.22502del , LRG_1028:g.22502del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.7184del MANE Select	ENSP00000357789.1:p.Ser2395ThrfsTer24
ENST00000368799.1:c.7184del	ENSP00000357789.1:p.Ser2395ThrfsTer24
NM_002016.1:c.7184del , LRG_1028t1:c.7184del	NP_002007.1:p.Ser2395ThrfsTer24
XM_011509329.1:c.7184del	XP_011507631.1:p.Ser2395ThrfsTer24
NM_002016.2:c.7184del MANE Select	NP_002007.1:p.Ser2395ThrfsTer24