Canonical Allele Identifier: CA2479947666
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304831_152304835delinsGTGTC , CM000663.2:g.152304831_152304835delinsGTGTC GRCh38
NC_000001.10:g.152277307_152277311delinsGTGTC , CM000663.1:g.152277307_152277311delinsGTGTC GRCh37
NC_000001.9:g.150543931_150543935delinsGTGTC NCBI36
NG_016190.1:g.25369_25373delinsGACAC , LRG_1028:g.25369_25373delinsGACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10051_10055delinsGACAC MANE Select ENSP00000357789.1:p.Asp3351=
ENST00000368799.1:c.10051_10055delinsGACAC ENSP00000357789.1:p.Asp3351=
NM_002016.1:c.10051_10055delinsGACAC , LRG_1028t1:c.10051_10055delinsGACAC NP_002007.1:p.Asp3351=
XM_011509329.1:c.9108+943_9108+947delinsGACAC XP_011507631.1:n.9108+943_9108+947delinsGACAC
NM_002016.2:c.10051_10055delinsGACAC MANE Select NP_002007.1:p.Asp3351=