Canonical Allele Identifier: CA342073487

Gene: FLG

Linked Data

• gnomAD v4: 1-152304831-G-A
• MyVariant Identifiers: chr1:g.152277307G>A (hg19) ; chr1:g.152304831G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304831G>A , CM000663.2:g.152304831G>A	GRCh38
NC_000001.10:g.152277307G>A , CM000663.1:g.152277307G>A	GRCh37
NC_000001.9:g.150543931G>A	NCBI36
NG_016190.1:g.25373C>T , LRG_1028:g.25373C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.10055C>T MANE Select	ENSP00000357789.1:p.Thr3352Ile
ENST00000368799.1:c.10055C>T	ENSP00000357789.1:p.Thr3352Ile
NM_002016.1:c.10055C>T , LRG_1028t1:c.10055C>T	NP_002007.1:p.Thr3352Ile
XM_011509329.1:c.9108+947C>T	XP_011507631.1:n.9108+947C>T
NM_002016.2:c.10055C>T MANE Select	NP_002007.1:p.Thr3352Ile