Canonical Allele Identifier: CA2479950133

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152309185_152309190delinsCCACCT , CM000663.2:g.152309185_152309190delinsCCACCT	GRCh38
NC_000001.10:g.152281661_152281666delinsCCACCT , CM000663.1:g.152281661_152281666delinsCCACCT	GRCh37
NC_000001.9:g.150548285_150548290delinsCCACCT	NCBI36
NG_016190.1:g.21014_21019delinsAGGTGG , LRG_1028:g.21014_21019delinsAGGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.5696_5701delinsAGGTGG MANE Select	ENSP00000357789.1:p.Gln1899=
ENST00000368799.1:c.5696_5701delinsAGGTGG	ENSP00000357789.1:p.Gln1899=
NM_002016.1:c.5696_5701delinsAGGTGG , LRG_1028t1:c.5696_5701delinsAGGTGG	NP_002007.1:p.Gln1899=
XM_011509329.1:c.5696_5701delinsAGGTGG	XP_011507631.1:p.Gln1899=
NM_002016.2:c.5696_5701delinsAGGTGG MANE Select	NP_002007.1:p.Gln1899=