Canonical Allele Identifier: CA342103904

Gene: FLG

Linked Data

• MyVariant Identifiers: chr1:g.152286379T>C (hg19) ; chr1:g.152313903T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152313903T>C , CM000663.2:g.152313903T>C	GRCh38
NC_000001.10:g.152286379T>C , CM000663.1:g.152286379T>C	GRCh37
NC_000001.9:g.150553003T>C	NCBI36
NG_016190.1:g.16301A>G , LRG_1028:g.16301A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000368799.2:c.983A>G MANE Select	ENSP00000357789.1:p.Gln328Arg
ENST00000368799.1:c.983A>G	ENSP00000357789.1:p.Gln328Arg
NM_002016.1:c.983A>G , LRG_1028t1:c.983A>G	NP_002007.1:p.Gln328Arg
NR_103778.1:n.445T>C
XM_011509329.1:c.983A>G	XP_011507631.1:p.Gln328Arg
NM_002016.2:c.983A>G MANE Select	NP_002007.1:p.Gln328Arg