Canonical Allele Identifier: CA2479951398

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152311498C= , CM000663.2:g.152311498C=	GRCh38
NC_000001.10:g.152283974C= , CM000663.1:g.152283974C=	GRCh37
NC_000001.9:g.150550598C=	NCBI36
NG_016190.1:g.18706G= , LRG_1028:g.18706G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.3388G= MANE Select	ENSP00000357789.1:p.Ala1130=
ENST00000368799.1:c.3388G=	ENSP00000357789.1:p.Ala1130=
NM_002016.1:c.3388G= , LRG_1028t1:c.3388G=	NP_002007.1:p.Ala1130=
XM_011509329.1:c.3388G=	XP_011507631.1:p.Ala1130=
NM_002016.2:c.3388G= MANE Select	NP_002007.1:p.Ala1130=