Canonical Allele Identifier: CA2647993659
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152309184_152309185insTGGA , CM000663.2:g.152309184_152309185insTGGA GRCh38
NC_000001.10:g.152281660_152281661insTGGA , CM000663.1:g.152281660_152281661insTGGA GRCh37
NC_000001.9:g.150548284_150548285insTGGA NCBI36
NG_016190.1:g.21019_21020insTCCA , LRG_1028:g.21019_21020insTCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5701_5702insTCCA MANE Select ENSP00000357789.1:p.Gly1901ValfsTer20
ENST00000368799.1:c.5701_5702insTCCA ENSP00000357789.1:p.Gly1901ValfsTer20
NM_002016.1:c.5701_5702insTCCA , LRG_1028t1:c.5701_5702insTCCA NP_002007.1:p.Gly1901ValfsTer20
XM_011509329.1:c.5701_5702insTCCA XP_011507631.1:p.Gly1901ValfsTer20
NM_002016.2:c.5701_5702insTCCA MANE Select NP_002007.1:p.Gly1901ValfsTer20