Canonical Allele Identifier: CA1105539

Gene: FLG

Linked Data

• ClinVar Variation Id: 2350646
• ClinVar RCV Id: RCV002964453
• dbSNP Id: rs536467375
• ExAC: 1:152281490 C / T
• gnomAD v2: 1-152281490-C-T
• gnomAD v3: 1-152309014-C-T
• gnomAD v4: 1-152309014-C-T
• COSMIC: COSM6292092
• MyVariant Identifiers: chr1:g.152281490C>T (hg19) ; chr1:g.152309014C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152309014C>T , CM000663.2:g.152309014C>T	GRCh38
NC_000001.10:g.152281490C>T , CM000663.1:g.152281490C>T	GRCh37
NC_000001.9:g.150548114C>T	NCBI36
NG_016190.1:g.21190G>A , LRG_1028:g.21190G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.5872G>A MANE Select	ENSP00000357789.1:p.Gly1958Arg
ENST00000368799.1:c.5872G>A	ENSP00000357789.1:p.Gly1958Arg
NM_002016.1:c.5872G>A , LRG_1028t1:c.5872G>A	NP_002007.1:p.Gly1958Arg
XM_011509329.1:c.5872G>A	XP_011507631.1:p.Gly1958Arg
NM_002016.2:c.5872G>A MANE Select	NP_002007.1:p.Gly1958Arg