Canonical Allele Identifier: CA2479947615
Gene: FLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304748_152304749delinsAC , CM000663.2:g.152304748_152304749delinsAC GRCh38
NC_000001.10:g.152277224_152277225delinsAC , CM000663.1:g.152277224_152277225delinsAC GRCh37
NC_000001.9:g.150543848_150543849delinsAC NCBI36
NG_016190.1:g.25455_25456delinsGT , LRG_1028:g.25455_25456delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.10137_10138delinsGT MANE Select ENSP00000357789.1:p.Arg3379=
ENST00000368799.1:c.10137_10138delinsGT ENSP00000357789.1:p.Arg3379=
NM_002016.1:c.10137_10138delinsGT , LRG_1028t1:c.10137_10138delinsGT NP_002007.1:p.Arg3379=
XM_011509329.1:c.9109-916_9109-915delinsGT XP_011507631.1:n.9109-916_9109-915delinsGT
NM_002016.2:c.10137_10138delinsGT MANE Select NP_002007.1:p.Arg3379=
Search 100 bp 5'
Search 100 bp 3'