Canonical Allele Identifier: CA420932250
Gene: FLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.152286477G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152314001G>A , CM000663.2:g.152314001G>A GRCh38
NC_000001.10:g.152286477G>A , CM000663.1:g.152286477G>A GRCh37
NC_000001.9:g.150553101G>A NCBI36
NG_016190.1:g.16203C>T , LRG_1028:g.16203C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.885C>T MANE Select ENSP00000357789.1:p.Ser295=
ENST00000368799.1:c.885C>T ENSP00000357789.1:p.Ser295=
NM_002016.1:c.885C>T , LRG_1028t1:c.885C>T NP_002007.1:p.Ser295=
NR_103778.1:n.543G>A
XM_011509329.1:c.885C>T XP_011507631.1:p.Ser295=
NM_002016.2:c.885C>T MANE Select NP_002007.1:p.Ser295=