Canonical Allele Identifier: CA1103475
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs773011736

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304678G>T , CM000663.2:g.152304678G>T GRCh38
NC_000001.10:g.152277154G>T , CM000663.1:g.152277154G>T GRCh37
NC_000001.9:g.150543778G>T NCBI36
NG_016190.1:g.25526C>A , LRG_1028:g.25526C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10208C>A MANE Select ENSP00000357789.1:p.Thr3403Asn
ENST00000368799.1:c.10208C>A ENSP00000357789.1:p.Thr3403Asn
NM_002016.1:c.10208C>A , LRG_1028t1:c.10208C>A NP_002007.1:p.Thr3403Asn
XM_011509329.1:c.9109-845C>A XP_011507631.1:n.9109-845C>A
NM_002016.2:c.10208C>A MANE Select NP_002007.1:p.Thr3403Asn