Canonical Allele Identifier: CA1144477662

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304852C= , CM000663.2:g.152304852C=	GRCh38
NC_000001.10:g.152277328C= , CM000663.1:g.152277328C=	GRCh37
NC_000001.9:g.150543952C=	NCBI36
NG_016190.1:g.25352G= , LRG_1028:g.25352G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.10034G= MANE Select	ENSP00000357789.1:p.Gly3345=
ENST00000368799.1:c.10034G=	ENSP00000357789.1:p.Gly3345=
NM_002016.1:c.10034G= , LRG_1028t1:c.10034G=	NP_002007.1:p.Gly3345=
XM_011509329.1:c.9108+926G=	XP_011507631.1:n.9108+926G=
NM_002016.2:c.10034G= MANE Select	NP_002007.1:p.Gly3345=