Canonical Allele Identifier: CA1103425
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs368372471

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304574G>A , CM000663.2:g.152304574G>A GRCh38
NC_000001.10:g.152277050G>A , CM000663.1:g.152277050G>A GRCh37
NC_000001.9:g.150543674G>A NCBI36
NG_016190.1:g.25630C>T , LRG_1028:g.25630C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.10312C>T MANE Select ENSP00000357789.1:p.Pro3438Ser
ENST00000368799.1:c.10312C>T ENSP00000357789.1:p.Pro3438Ser
NM_002016.1:c.10312C>T , LRG_1028t1:c.10312C>T NP_002007.1:p.Pro3438Ser
XM_011509329.1:c.9109-741C>T XP_011507631.1:n.9109-741C>T
NM_002016.2:c.10312C>T MANE Select NP_002007.1:p.Pro3438Ser