Canonical Allele Identifier: CA1105337
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs771088791

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152308632C>G , CM000663.2:g.152308632C>G GRCh38
NC_000001.10:g.152281108C>G , CM000663.1:g.152281108C>G GRCh37
NC_000001.9:g.150547732C>G NCBI36
NG_016190.1:g.21572G>C , LRG_1028:g.21572G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.6254G>C MANE Select ENSP00000357789.1:p.Gly2085Ala
ENST00000368799.1:c.6254G>C ENSP00000357789.1:p.Gly2085Ala
NM_002016.1:c.6254G>C , LRG_1028t1:c.6254G>C NP_002007.1:p.Gly2085Ala
XM_011509329.1:c.6254G>C XP_011507631.1:p.Gly2085Ala
NM_002016.2:c.6254G>C MANE Select NP_002007.1:p.Gly2085Ala