Canonical Allele Identifier: CA420929413

Gene: FLG

Linked Data

• gnomAD v4: 1-152309219-G-T
• MyVariant Identifiers: chr1:g.152281695G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152309219G>T , CM000663.2:g.152309219G>T	GRCh38
NC_000001.10:g.152281695G>T , CM000663.1:g.152281695G>T	GRCh37
NC_000001.9:g.150548319G>T	NCBI36
NG_016190.1:g.20985C>A , LRG_1028:g.20985C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.5667C>A MANE Select	ENSP00000357789.1:p.Ser1889=
ENST00000368799.1:c.5667C>A	ENSP00000357789.1:p.Ser1889=
NM_002016.1:c.5667C>A , LRG_1028t1:c.5667C>A	NP_002007.1:p.Ser1889=
XM_011509329.1:c.5667C>A	XP_011507631.1:p.Ser1889=
NM_002016.2:c.5667C>A MANE Select	NP_002007.1:p.Ser1889=