Canonical Allele Identifier: CA2647993622

Gene: FLG

Linked Data

• gnomAD v4: 1-152311095-C-CCGA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152311095_152311096insCGA , CM000663.2:g.152311095_152311096insCGA	GRCh38
NC_000001.10:g.152283571_152283572insCGA , CM000663.1:g.152283571_152283572insCGA	GRCh37
NC_000001.9:g.150550195_150550196insCGA	NCBI36
NG_016190.1:g.19108_19109insTCG , LRG_1028:g.19108_19109insTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.3790_3791insTCG MANE Select	ENSP00000357789.1:p.Arg1264delinsIleGly
ENST00000368799.1:c.3790_3791insTCG	ENSP00000357789.1:p.Arg1264delinsIleGly
NM_002016.1:c.3790_3791insTCG , LRG_1028t1:c.3790_3791insTCG	NP_002007.1:p.Arg1264delinsIleGly
XM_011509329.1:c.3790_3791insTCG	XP_011507631.1:p.Arg1264delinsIleGly
NM_002016.2:c.3790_3791insTCG MANE Select	NP_002007.1:p.Arg1264delinsIleGly