Canonical Allele Identifier: CA2479950144
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152309195_152309196delinsGT , CM000663.2:g.152309195_152309196delinsGT GRCh38
NC_000001.10:g.152281671_152281672delinsGT , CM000663.1:g.152281671_152281672delinsGT GRCh37
NC_000001.9:g.150548295_150548296delinsGT NCBI36
NG_016190.1:g.21008_21009delinsAC , LRG_1028:g.21008_21009delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5690_5691delinsAC MANE Select ENSP00000357789.1:p.His1897=
ENST00000368799.1:c.5690_5691delinsAC ENSP00000357789.1:p.His1897=
NM_002016.1:c.5690_5691delinsAC , LRG_1028t1:c.5690_5691delinsAC NP_002007.1:p.His1897=
XM_011509329.1:c.5690_5691delinsAC XP_011507631.1:p.His1897=
NM_002016.2:c.5690_5691delinsAC MANE Select NP_002007.1:p.His1897=