Canonical Allele Identifier: CA420931957

Gene: FLG

Linked Data

• MyVariant Identifiers: chr1:g.152286372T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152313896T>C , CM000663.2:g.152313896T>C	GRCh38
NC_000001.10:g.152286372T>C , CM000663.1:g.152286372T>C	GRCh37
NC_000001.9:g.150552996T>C	NCBI36
NG_016190.1:g.16308A>G , LRG_1028:g.16308A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000368799.2:c.990A>G MANE Select	ENSP00000357789.1:p.Arg330=
ENST00000368799.1:c.990A>G	ENSP00000357789.1:p.Arg330=
NM_002016.1:c.990A>G , LRG_1028t1:c.990A>G	NP_002007.1:p.Arg330=
NR_103778.1:n.438T>C
XM_011509329.1:c.990A>G	XP_011507631.1:p.Arg330=
NM_002016.2:c.990A>G MANE Select	NP_002007.1:p.Arg330=