Canonical Allele Identifier: CA342055821
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152308731T>C , CM000663.2:g.152308731T>C GRCh38
NC_000001.10:g.152281207T>C , CM000663.1:g.152281207T>C GRCh37
NC_000001.9:g.150547831T>C NCBI36
NG_016190.1:g.21473A>G , LRG_1028:g.21473A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.6155A>G MANE Select ENSP00000357789.1:p.Glu2052Gly
ENST00000368799.1:c.6155A>G ENSP00000357789.1:p.Glu2052Gly
NM_002016.1:c.6155A>G , LRG_1028t1:c.6155A>G NP_002007.1:p.Glu2052Gly
XM_011509329.1:c.6155A>G XP_011507631.1:p.Glu2052Gly
NM_002016.2:c.6155A>G MANE Select NP_002007.1:p.Glu2052Gly