Canonical Allele Identifier: CA2479951943
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312499_152312503delinsTGGTA , CM000663.2:g.152312499_152312503delinsTGGTA GRCh38
NC_000001.10:g.152284975_152284979delinsTGGTA , CM000663.1:g.152284975_152284979delinsTGGTA GRCh37
NC_000001.9:g.150551599_150551603delinsTGGTA NCBI36
NG_016190.1:g.17701_17705delinsTACCA , LRG_1028:g.17701_17705delinsTACCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2383_2387delinsTACCA MANE Select ENSP00000357789.1:p.Tyr795=
ENST00000368799.1:c.2383_2387delinsTACCA ENSP00000357789.1:p.Tyr795=
NM_002016.1:c.2383_2387delinsTACCA , LRG_1028t1:c.2383_2387delinsTACCA NP_002007.1:p.Tyr795=
XM_011509329.1:c.2383_2387delinsTACCA XP_011507631.1:p.Tyr795=
NM_002016.2:c.2383_2387delinsTACCA MANE Select NP_002007.1:p.Tyr795=