Canonical Allele Identifier: CA1106478
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs139579576

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311012T>C , CM000663.2:g.152311012T>C GRCh38
NC_000001.10:g.152283488T>C , CM000663.1:g.152283488T>C GRCh37
NC_000001.9:g.150550112T>C NCBI36
NG_016190.1:g.19192A>G , LRG_1028:g.19192A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.3874A>G MANE Select ENSP00000357789.1:p.Arg1292Gly
ENST00000368799.1:c.3874A>G ENSP00000357789.1:p.Arg1292Gly
NM_002016.1:c.3874A>G , LRG_1028t1:c.3874A>G NP_002007.1:p.Arg1292Gly
XM_011509329.1:c.3874A>G XP_011507631.1:p.Arg1292Gly
NM_002016.2:c.3874A>G MANE Select NP_002007.1:p.Arg1292Gly