Canonical Allele Identifier: CA1144625378

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304686A= , CM000663.2:g.152304686A=	GRCh38
NC_000001.10:g.152277162A= , CM000663.1:g.152277162A=	GRCh37
NC_000001.9:g.150543786A=	NCBI36
NG_016190.1:g.25518T= , LRG_1028:g.25518T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.10200T= MANE Select	ENSP00000357789.1:p.His3400=
ENST00000368799.1:c.10200T=	ENSP00000357789.1:p.His3400=
NM_002016.1:c.10200T= , LRG_1028t1:c.10200T=	NP_002007.1:p.His3400=
XM_011509329.1:c.9109-853T=	XP_011507631.1:n.9109-853T=
NM_002016.2:c.10200T= MANE Select	NP_002007.1:p.His3400=