Canonical Allele Identifier: CA342074755

Gene: FLG

Linked Data

• MyVariant Identifiers: chr1:g.152277458G>T (hg19) ; chr1:g.152304982G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304982G>T , CM000663.2:g.152304982G>T	GRCh38
NC_000001.10:g.152277458G>T , CM000663.1:g.152277458G>T	GRCh37
NC_000001.9:g.150544082G>T	NCBI36
NG_016190.1:g.25222C>A , LRG_1028:g.25222C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.9904C>A MANE Select	ENSP00000357789.1:p.His3302Asn
ENST00000368799.1:c.9904C>A	ENSP00000357789.1:p.His3302Asn
NM_002016.1:c.9904C>A , LRG_1028t1:c.9904C>A	NP_002007.1:p.His3302Asn
XM_011509329.1:c.9108+796C>A	XP_011507631.1:n.9108+796C>A
NM_002016.2:c.9904C>A MANE Select	NP_002007.1:p.His3302Asn