Canonical Allele Identifier: CA1106445

Gene: FLG

Linked Data

• dbSNP Id: rs772787336
• ExAC: 1:152283435 A / T
• gnomAD v2: 1-152283435-A-T
• MyVariant Identifiers: chr1:g.152283435A>T (hg19) ; chr1:g.152310959A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152310959A>T , CM000663.2:g.152310959A>T	GRCh38
NC_000001.10:g.152283435A>T , CM000663.1:g.152283435A>T	GRCh37
NC_000001.9:g.150550059A>T	NCBI36
NG_016190.1:g.19245T>A , LRG_1028:g.19245T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368799.2:c.3927T>A MANE Select	ENSP00000357789.1:p.Pro1309=
ENST00000368799.1:c.3927T>A	ENSP00000357789.1:p.Pro1309=
NM_002016.1:c.3927T>A , LRG_1028t1:c.3927T>A	NP_002007.1:p.Pro1309=
XM_011509329.1:c.3927T>A	XP_011507631.1:p.Pro1309=
NM_002016.2:c.3927T>A MANE Select	NP_002007.1:p.Pro1309=