Canonical Allele Identifier: CA2573904872

Gene: FLG

Linked Data

• dbSNP Id: rs2101649857

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152312319_152312320insTGG , CM000663.2:g.152312319_152312320insTGG	GRCh38
NC_000001.10:g.152284795_152284796insTGG , CM000663.1:g.152284795_152284796insTGG	GRCh37
NC_000001.9:g.150551419_150551420insTGG	NCBI36
NG_016190.1:g.17884_17885insCCA , LRG_1028:g.17884_17885insCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.2566_2567insCCA MANE Select	ENSP00000357789.1:p.His856delinsProAsn
ENST00000368799.1:c.2566_2567insCCA	ENSP00000357789.1:p.His856delinsProAsn
NM_002016.1:c.2566_2567insCCA , LRG_1028t1:c.2566_2567insCCA	NP_002007.1:p.His856delinsProAsn
XM_011509329.1:c.2566_2567insCCA	XP_011507631.1:p.His856delinsProAsn
NM_002016.2:c.2566_2567insCCA MANE Select	NP_002007.1:p.His856delinsProAsn