Canonical Allele Identifier: CA342071858

Gene: FLG

Linked Data

• dbSNP Id: rs368519093
• MyVariant Identifiers: chr1:g.152282618C>T (hg19) ; chr1:g.152310142C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152310142C>T , CM000663.2:g.152310142C>T	GRCh38
NC_000001.10:g.152282618C>T , CM000663.1:g.152282618C>T	GRCh37
NC_000001.9:g.150549242C>T	NCBI36
NG_016190.1:g.20062G>A , LRG_1028:g.20062G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.4744G>A MANE Select	ENSP00000357789.1:p.Ala1582Thr
ENST00000368799.1:c.4744G>A	ENSP00000357789.1:p.Ala1582Thr
NM_002016.1:c.4744G>A , LRG_1028t1:c.4744G>A	NP_002007.1:p.Ala1582Thr
XM_011509329.1:c.4744G>A	XP_011507631.1:p.Ala1582Thr
NM_002016.2:c.4744G>A MANE Select	NP_002007.1:p.Ala1582Thr