Canonical Allele Identifier: CA1142111275

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304262C= , CM000663.2:g.152304262C=	GRCh38
NC_000001.10:g.152276738C= , CM000663.1:g.152276738C=	GRCh37
NC_000001.9:g.150543362C=	NCBI36
NG_016190.1:g.25942G= , LRG_1028:g.25942G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.10624G= MANE Select	ENSP00000357789.1:p.Asp3542=
ENST00000368799.1:c.10624G=	ENSP00000357789.1:p.Asp3542=
NM_002016.1:c.10624G= , LRG_1028t1:c.10624G=	NP_002007.1:p.Asp3542=
XM_011509329.1:c.9109-429G=	XP_011507631.1:n.9109-429G=
NM_002016.2:c.10624G= MANE Select	NP_002007.1:p.Asp3542=