Canonical Allele Identifier: CA342072627

Gene: FLG

Linked Data

• gnomAD v4: 1-152304685-C-T
• MyVariant Identifiers: chr1:g.152277161C>T (hg19) ; chr1:g.152304685C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304685C>T , CM000663.2:g.152304685C>T	GRCh38
NC_000001.10:g.152277161C>T , CM000663.1:g.152277161C>T	GRCh37
NC_000001.9:g.150543785C>T	NCBI36
NG_016190.1:g.25519G>A , LRG_1028:g.25519G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.10201G>A MANE Select	ENSP00000357789.1:p.Gly3401Arg
ENST00000368799.1:c.10201G>A	ENSP00000357789.1:p.Gly3401Arg
NM_002016.1:c.10201G>A , LRG_1028t1:c.10201G>A	NP_002007.1:p.Gly3401Arg
XM_011509329.1:c.9109-852G>A	XP_011507631.1:n.9109-852G>A
NM_002016.2:c.10201G>A MANE Select	NP_002007.1:p.Gly3401Arg