Canonical Allele Identifier: CA342073699

Gene: FLG

Linked Data

• MyVariant Identifiers: chr1:g.152277329C>G (hg19) ; chr1:g.152304853C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304853C>G , CM000663.2:g.152304853C>G	GRCh38
NC_000001.10:g.152277329C>G , CM000663.1:g.152277329C>G	GRCh37
NC_000001.9:g.150543953C>G	NCBI36
NG_016190.1:g.25351G>C , LRG_1028:g.25351G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000368799.2:c.10033G>C MANE Select	ENSP00000357789.1:p.Gly3345Arg
ENST00000368799.1:c.10033G>C	ENSP00000357789.1:p.Gly3345Arg
NM_002016.1:c.10033G>C , LRG_1028t1:c.10033G>C	NP_002007.1:p.Gly3345Arg
XM_011509329.1:c.9108+925G>C	XP_011507631.1:n.9108+925G>C
NM_002016.2:c.10033G>C MANE Select	NP_002007.1:p.Gly3345Arg