Canonical Allele Identifier: CA342062251

Gene: FLG

Linked Data

• dbSNP Id: rs1393401596
• MyVariant Identifiers: chr1:g.152281699G>A (hg19) ; chr1:g.152309223G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152309223G>A , CM000663.2:g.152309223G>A	GRCh38
NC_000001.10:g.152281699G>A , CM000663.1:g.152281699G>A	GRCh37
NC_000001.9:g.150548323G>A	NCBI36
NG_016190.1:g.20981C>T , LRG_1028:g.20981C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.5663C>T MANE Select	ENSP00000357789.1:p.Ala1888Val
ENST00000368799.1:c.5663C>T	ENSP00000357789.1:p.Ala1888Val
NM_002016.1:c.5663C>T , LRG_1028t1:c.5663C>T	NP_002007.1:p.Ala1888Val
XM_011509329.1:c.5663C>T	XP_011507631.1:p.Ala1888Val
NM_002016.2:c.5663C>T MANE Select	NP_002007.1:p.Ala1888Val