Canonical Allele Identifier: CA420931250

Gene: FLG

Linked Data

• gnomAD v4: 1-152311547-A-G
• MyVariant Identifiers: chr1:g.152284023A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152311547A>G , CM000663.2:g.152311547A>G	GRCh38
NC_000001.10:g.152284023A>G , CM000663.1:g.152284023A>G	GRCh37
NC_000001.9:g.150550647A>G	NCBI36
NG_016190.1:g.18657T>C , LRG_1028:g.18657T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.3339T>C MANE Select	ENSP00000357789.1:p.Arg1113=
ENST00000368799.1:c.3339T>C	ENSP00000357789.1:p.Arg1113=
NM_002016.1:c.3339T>C , LRG_1028t1:c.3339T>C	NP_002007.1:p.Arg1113=
XM_011509329.1:c.3339T>C	XP_011507631.1:p.Arg1113=
NM_002016.2:c.3339T>C MANE Select	NP_002007.1:p.Arg1113=