Canonical Allele Identifier: CA342076657

Gene: FLG

Linked Data

• gnomAD v4: 1-152310692-A-T
• MyVariant Identifiers: chr1:g.152283168A>T (hg19) ; chr1:g.152310692A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152310692A>T , CM000663.2:g.152310692A>T	GRCh38
NC_000001.10:g.152283168A>T , CM000663.1:g.152283168A>T	GRCh37
NC_000001.9:g.150549792A>T	NCBI36
NG_016190.1:g.19512T>A , LRG_1028:g.19512T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368799.2:c.4194T>A MANE Select	ENSP00000357789.1:p.Ser1398Arg
ENST00000368799.1:c.4194T>A	ENSP00000357789.1:p.Ser1398Arg
NM_002016.1:c.4194T>A , LRG_1028t1:c.4194T>A	NP_002007.1:p.Ser1398Arg
XM_011509329.1:c.4194T>A	XP_011507631.1:p.Ser1398Arg
NM_002016.2:c.4194T>A MANE Select	NP_002007.1:p.Ser1398Arg