Canonical Allele Identifier: CA2479951818
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312243_152312244delinsAT , CM000663.2:g.152312243_152312244delinsAT GRCh38
NC_000001.10:g.152284719_152284720delinsAT , CM000663.1:g.152284719_152284720delinsAT GRCh37
NC_000001.9:g.150551343_150551344delinsAT NCBI36
NG_016190.1:g.17960_17961delinsAT , LRG_1028:g.17960_17961delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2642_2643delinsAT MANE Select ENSP00000357789.1:p.Asp881=
ENST00000368799.1:c.2642_2643delinsAT ENSP00000357789.1:p.Asp881=
NM_002016.1:c.2642_2643delinsAT , LRG_1028t1:c.2642_2643delinsAT NP_002007.1:p.Asp881=
XM_011509329.1:c.2642_2643delinsAT XP_011507631.1:p.Asp881=
NM_002016.2:c.2642_2643delinsAT MANE Select NP_002007.1:p.Asp881=