Canonical Allele Identifier: CA420932269
Gene: FLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.152286486A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152314010A>T , CM000663.2:g.152314010A>T GRCh38
NC_000001.10:g.152286486A>T , CM000663.1:g.152286486A>T GRCh37
NC_000001.9:g.150553110A>T NCBI36
NG_016190.1:g.16194T>A , LRG_1028:g.16194T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.876T>A MANE Select ENSP00000357789.1:p.Arg292=
ENST00000368799.1:c.876T>A ENSP00000357789.1:p.Arg292=
NM_002016.1:c.876T>A , LRG_1028t1:c.876T>A NP_002007.1:p.Arg292=
NR_103778.1:n.552A>T
XM_011509329.1:c.876T>A XP_011507631.1:p.Arg292=
NM_002016.2:c.876T>A MANE Select NP_002007.1:p.Arg292=