Canonical Allele Identifier: CA1104847
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs761842201
ExAC: 1:152280144 T / TTCC
gnomAD v2: 1-152280144-T-TTCC
gnomAD v3: 1-152307668-T-TTCC
gnomAD v4: 1-152307668-T-TTCC
MyVariant Identifiers: chr1:g.152280144_152280145insTCC (hg19) chr1:g.152307668_152307669insTCC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152307668_152307669insTCC , CM000663.2:g.152307668_152307669insTCC GRCh38
NC_000001.10:g.152280144_152280145insTCC , CM000663.1:g.152280144_152280145insTCC GRCh37
NC_000001.9:g.150546768_150546769insTCC NCBI36
NG_016190.1:g.22535_22536insGGA , LRG_1028:g.22535_22536insGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.7217_7218insGGA MANE Select ENSP00000357789.1:p.Gly2406_Arg2407insGlu
ENST00000368799.1:c.7217_7218insGGA ENSP00000357789.1:p.Gly2406_Arg2407insGlu
NM_002016.1:c.7217_7218insGGA , LRG_1028t1:c.7217_7218insGGA NP_002007.1:p.Gly2406_Arg2407insGlu
XM_011509329.1:c.7217_7218insGGA XP_011507631.1:p.Gly2406_Arg2407insGlu
NM_002016.2:c.7217_7218insGGA MANE Select NP_002007.1:p.Gly2406_Arg2407insGlu
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