Canonical Allele Identifier: CA2479950137

Gene: FLG

Linked Data

• dbSNP Id: rs1652209648

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152309188_152309189insTGGA , CM000663.2:g.152309188_152309189insTGGA	GRCh38
NC_000001.10:g.152281664_152281665insTGGA , CM000663.1:g.152281664_152281665insTGGA	GRCh37
NC_000001.9:g.150548288_150548289insTGGA	NCBI36
NG_016190.1:g.21015_21016insTCCA , LRG_1028:g.21015_21016insTCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.5697_5698insTCCA MANE Select	ENSP00000357789.1:p.Val1900SerfsTer21
ENST00000368799.1:c.5697_5698insTCCA	ENSP00000357789.1:p.Val1900SerfsTer21
NM_002016.1:c.5697_5698insTCCA , LRG_1028t1:c.5697_5698insTCCA	NP_002007.1:p.Val1900SerfsTer21
XM_011509329.1:c.5697_5698insTCCA	XP_011507631.1:p.Val1900SerfsTer21
NM_002016.2:c.5697_5698insTCCA MANE Select	NP_002007.1:p.Val1900SerfsTer21