Canonical Allele Identifier: CA2479947573
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304676_152304677delinsTG , CM000663.2:g.152304676_152304677delinsTG GRCh38
NC_000001.10:g.152277152_152277153delinsTG , CM000663.1:g.152277152_152277153delinsTG GRCh37
NC_000001.9:g.150543776_150543777delinsTG NCBI36
NG_016190.1:g.25527_25528delinsCA , LRG_1028:g.25527_25528delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10209_10210delinsCA MANE Select ENSP00000357789.1:p.Thr3403=
ENST00000368799.1:c.10209_10210delinsCA ENSP00000357789.1:p.Thr3403=
NM_002016.1:c.10209_10210delinsCA , LRG_1028t1:c.10209_10210delinsCA NP_002007.1:p.Thr3403=
XM_011509329.1:c.9109-844_9109-843delinsCA XP_011507631.1:n.9109-844_9109-843delinsCA
NM_002016.2:c.10209_10210delinsCA MANE Select NP_002007.1:p.Thr3403=