Canonical Allele Identifier: CA526662116

Gene: FLG

Linked Data

• dbSNP Id: rs1570894677
• gnomAD v2: 1-152276885-C-CCTT
• gnomAD v3: 1-152304409-C-CCTT
• gnomAD v4: 1-152304409-C-CCTT
• MyVariant Identifiers: chr1:g.152276885_152276886insCTT (hg19) ; chr1:g.152304409_152304410insCTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304409_152304410insCTT , CM000663.2:g.152304409_152304410insCTT	GRCh38
NC_000001.10:g.152276885_152276886insCTT , CM000663.1:g.152276885_152276886insCTT	GRCh37
NC_000001.9:g.150543509_150543510insCTT	NCBI36
NG_016190.1:g.25794_25795insAAG , LRG_1028:g.25794_25795insAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.10476_10477insAAG MANE Select	ENSP00000357789.1:p.Asp3492_Glu3493insLys
ENST00000368799.1:c.10476_10477insAAG	ENSP00000357789.1:p.Asp3492_Glu3493insLys
NM_002016.1:c.10476_10477insAAG , LRG_1028t1:c.10476_10477insAAG	NP_002007.1:p.Asp3492_Glu3493insLys
XM_011509329.1:c.9109-577_9109-576insAAG	XP_011507631.1:n.9109-577_9109-576insAAG
NM_002016.2:c.10476_10477insAAG MANE Select	NP_002007.1:p.Asp3492_Glu3493insLys