Canonical Allele Identifier: CA1144132038

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304249T= , CM000663.2:g.152304249T=	GRCh38
NC_000001.10:g.152276725T= , CM000663.1:g.152276725T=	GRCh37
NC_000001.9:g.150543349T=	NCBI36
NG_016190.1:g.25955A= , LRG_1028:g.25955A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.10637A= MANE Select	ENSP00000357789.1:p.Gln3546=
ENST00000368799.1:c.10637A=	ENSP00000357789.1:p.Gln3546=
NM_002016.1:c.10637A= , LRG_1028t1:c.10637A=	NP_002007.1:p.Gln3546=
XM_011509329.1:c.9109-416A=	XP_011507631.1:n.9109-416A=
NM_002016.2:c.10637A= MANE Select	NP_002007.1:p.Gln3546=