Canonical Allele Identifier: CA2479950855
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152310955_152310956delinsAC , CM000663.2:g.152310955_152310956delinsAC GRCh38
NC_000001.10:g.152283431_152283432delinsAC , CM000663.1:g.152283431_152283432delinsAC GRCh37
NC_000001.9:g.150550055_150550056delinsAC NCBI36
NG_016190.1:g.19248_19249delinsGT , LRG_1028:g.19248_19249delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.3930_3931delinsGT MANE Select ENSP00000357789.1:p.Gly1310=
ENST00000368799.1:c.3930_3931delinsGT ENSP00000357789.1:p.Gly1310=
NM_002016.1:c.3930_3931delinsGT , LRG_1028t1:c.3930_3931delinsGT NP_002007.1:p.Gly1310=
XM_011509329.1:c.3930_3931delinsGT XP_011507631.1:p.Gly1310=
NM_002016.2:c.3930_3931delinsGT MANE Select NP_002007.1:p.Gly1310=