Canonical Allele Identifier: CA2479949263
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152307670_152307671delinsCT , CM000663.2:g.152307670_152307671delinsCT GRCh38
NC_000001.10:g.152280146_152280147delinsCT , CM000663.1:g.152280146_152280147delinsCT GRCh37
NC_000001.9:g.150546770_150546771delinsCT NCBI36
NG_016190.1:g.22533_22534delinsAG , LRG_1028:g.22533_22534delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.7215_7216delinsAG MANE Select ENSP00000357789.1:p.Ala2405=
ENST00000368799.1:c.7215_7216delinsAG ENSP00000357789.1:p.Ala2405=
NM_002016.1:c.7215_7216delinsAG , LRG_1028t1:c.7215_7216delinsAG NP_002007.1:p.Ala2405=
XM_011509329.1:c.7215_7216delinsAG XP_011507631.1:p.Ala2405=
NM_002016.2:c.7215_7216delinsAG MANE Select NP_002007.1:p.Ala2405=