Canonical Allele Identifier: CA342073638
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304848A>C , CM000663.2:g.152304848A>C GRCh38
NC_000001.10:g.152277324A>C , CM000663.1:g.152277324A>C GRCh37
NC_000001.9:g.150543948A>C NCBI36
NG_016190.1:g.25356T>G , LRG_1028:g.25356T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.10038T>G MANE Select ENSP00000357789.1:p.His3346Gln
ENST00000368799.1:c.10038T>G ENSP00000357789.1:p.His3346Gln
NM_002016.1:c.10038T>G , LRG_1028t1:c.10038T>G NP_002007.1:p.His3346Gln
XM_011509329.1:c.9108+930T>G XP_011507631.1:n.9108+930T>G
NM_002016.2:c.10038T>G MANE Select NP_002007.1:p.His3346Gln