Canonical Allele Identifier: CA2479949759
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152308650_152308651delinsTG , CM000663.2:g.152308650_152308651delinsTG GRCh38
NC_000001.10:g.152281126_152281127delinsTG , CM000663.1:g.152281126_152281127delinsTG GRCh37
NC_000001.9:g.150547750_150547751delinsTG NCBI36
NG_016190.1:g.21553_21554delinsCA , LRG_1028:g.21553_21554delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.6235_6236delinsCA MANE Select ENSP00000357789.1:p.Gln2079=
ENST00000368799.1:c.6235_6236delinsCA ENSP00000357789.1:p.Gln2079=
NM_002016.1:c.6235_6236delinsCA , LRG_1028t1:c.6235_6236delinsCA NP_002007.1:p.Gln2079=
XM_011509329.1:c.6235_6236delinsCA XP_011507631.1:p.Gln2079=
NM_002016.2:c.6235_6236delinsCA MANE Select NP_002007.1:p.Gln2079=