Canonical Allele Identifier: CA342103830
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152313889A>G , CM000663.2:g.152313889A>G GRCh38
NC_000001.10:g.152286365A>G , CM000663.1:g.152286365A>G GRCh37
NC_000001.9:g.150552989A>G NCBI36
NG_016190.1:g.16315T>C , LRG_1028:g.16315T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.997T>C MANE Select ENSP00000357789.1:p.Ser333Pro
ENST00000368799.1:c.997T>C ENSP00000357789.1:p.Ser333Pro
NM_002016.1:c.997T>C , LRG_1028t1:c.997T>C NP_002007.1:p.Ser333Pro
NR_103778.1:n.431A>G
XM_011509329.1:c.997T>C XP_011507631.1:p.Ser333Pro
NM_002016.2:c.997T>C MANE Select NP_002007.1:p.Ser333Pro