Canonical Allele Identifier: CA645521847
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312399_152312400delinsTT , CM000663.2:g.152312399_152312400delinsTT GRCh38
NC_000001.10:g.152284875_152284876delinsTT , CM000663.1:g.152284875_152284876delinsTT GRCh37
NC_000001.9:g.150551499_150551500delinsTT NCBI36
NG_016190.1:g.17804_17805delinsAA , LRG_1028:g.17804_17805delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2486_2487delinsAA MANE Select ENSP00000357789.1:p.Ser829Ter
ENST00000368799.1:c.2486_2487delinsAA ENSP00000357789.1:p.Ser829Ter
NM_002016.1:c.2486_2487delinsAA , LRG_1028t1:c.2486_2487delinsAA NP_002007.1:p.Ser829Ter
XM_011509329.1:c.2486_2487delinsAA XP_011507631.1:p.Ser829Ter
NM_002016.2:c.2486_2487delinsAA MANE Select NP_002007.1:p.Ser829Ter