Canonical Allele Identifier: CA1148413801

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152308684_152308687delinsGGGG , CM000663.2:g.152308684_152308687delinsGGGG	GRCh38
NC_000001.10:g.152281160_152281163delinsGGGG , CM000663.1:g.152281160_152281163delinsGGGG	GRCh37
NC_000001.9:g.150547784_150547787delinsGGGG	NCBI36
NG_016190.1:g.21517_21520delinsCCCC , LRG_1028:g.21517_21520delinsCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.6199_6202delinsCCCC MANE Select	ENSP00000357789.1:p.Pro2067=
ENST00000368799.1:c.6199_6202delinsCCCC	ENSP00000357789.1:p.Pro2067=
NM_002016.1:c.6199_6202delinsCCCC , LRG_1028t1:c.6199_6202delinsCCCC	NP_002007.1:p.Pro2067=
XM_011509329.1:c.6199_6202delinsCCCC	XP_011507631.1:p.Pro2067=
NM_002016.2:c.6199_6202delinsCCCC MANE Select	NP_002007.1:p.Pro2067=