Canonical Allele Identifier: CA420926654
Gene: FLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.152277137G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304661G>T , CM000663.2:g.152304661G>T GRCh38
NC_000001.10:g.152277137G>T , CM000663.1:g.152277137G>T GRCh37
NC_000001.9:g.150543761G>T NCBI36
NG_016190.1:g.25543C>A , LRG_1028:g.25543C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.10225C>A MANE Select ENSP00000357789.1:p.Arg3409=
ENST00000368799.1:c.10225C>A ENSP00000357789.1:p.Arg3409=
NM_002016.1:c.10225C>A , LRG_1028t1:c.10225C>A NP_002007.1:p.Arg3409=
XM_011509329.1:c.9109-828C>A XP_011507631.1:n.9109-828C>A
NM_002016.2:c.10225C>A MANE Select NP_002007.1:p.Arg3409=