Canonical Allele Identifier: CA420926886
Gene: FLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.152277042T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304566T>A , CM000663.2:g.152304566T>A GRCh38
NC_000001.10:g.152277042T>A , CM000663.1:g.152277042T>A GRCh37
NC_000001.9:g.150543666T>A NCBI36
NG_016190.1:g.25638A>T , LRG_1028:g.25638A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.10320A>T MANE Select ENSP00000357789.1:p.Ser3440=
ENST00000368799.1:c.10320A>T ENSP00000357789.1:p.Ser3440=
NM_002016.1:c.10320A>T , LRG_1028t1:c.10320A>T NP_002007.1:p.Ser3440=
XM_011509329.1:c.9109-733A>T XP_011507631.1:n.9109-733A>T
NM_002016.2:c.10320A>T MANE Select NP_002007.1:p.Ser3440=