Canonical Allele Identifier: CA342080863
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311053C>T , CM000663.2:g.152311053C>T GRCh38
NC_000001.10:g.152283529C>T , CM000663.1:g.152283529C>T GRCh37
NC_000001.9:g.150550153C>T NCBI36
NG_016190.1:g.19151G>A , LRG_1028:g.19151G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.3833G>A MANE Select ENSP00000357789.1:p.Arg1278Lys
ENST00000368799.1:c.3833G>A ENSP00000357789.1:p.Arg1278Lys
NM_002016.1:c.3833G>A , LRG_1028t1:c.3833G>A NP_002007.1:p.Arg1278Lys
XM_011509329.1:c.3833G>A XP_011507631.1:p.Arg1278Lys
NM_002016.2:c.3833G>A MANE Select NP_002007.1:p.Arg1278Lys