Canonical Allele Identifier: CA342076665

Gene: FLG

Linked Data

• gnomAD v4: 1-152310693-C-G
• MyVariant Identifiers: chr1:g.152283169C>G (hg19) ; chr1:g.152310693C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152310693C>G , CM000663.2:g.152310693C>G	GRCh38
NC_000001.10:g.152283169C>G , CM000663.1:g.152283169C>G	GRCh37
NC_000001.9:g.150549793C>G	NCBI36
NG_016190.1:g.19511G>C , LRG_1028:g.19511G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000368799.2:c.4193G>C MANE Select	ENSP00000357789.1:p.Ser1398Thr
ENST00000368799.1:c.4193G>C	ENSP00000357789.1:p.Ser1398Thr
NM_002016.1:c.4193G>C , LRG_1028t1:c.4193G>C	NP_002007.1:p.Ser1398Thr
XM_011509329.1:c.4193G>C	XP_011507631.1:p.Ser1398Thr
NM_002016.2:c.4193G>C MANE Select	NP_002007.1:p.Ser1398Thr