Canonical Allele Identifier: CA342049278
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152307777T>G , CM000663.2:g.152307777T>G GRCh38
NC_000001.10:g.152280253T>G , CM000663.1:g.152280253T>G GRCh37
NC_000001.9:g.150546877T>G NCBI36
NG_016190.1:g.22427A>C , LRG_1028:g.22427A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.7109A>C MANE Select ENSP00000357789.1:p.Asp2370Ala
ENST00000368799.1:c.7109A>C ENSP00000357789.1:p.Asp2370Ala
NM_002016.1:c.7109A>C , LRG_1028t1:c.7109A>C NP_002007.1:p.Asp2370Ala
XM_011509329.1:c.7109A>C XP_011507631.1:p.Asp2370Ala
NM_002016.2:c.7109A>C MANE Select NP_002007.1:p.Asp2370Ala