Canonical Allele Identifier: CA2479947759

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304991_152304992delinsCT , CM000663.2:g.152304991_152304992delinsCT	GRCh38
NC_000001.10:g.152277467_152277468delinsCT , CM000663.1:g.152277467_152277468delinsCT	GRCh37
NC_000001.9:g.150544091_150544092delinsCT	NCBI36
NG_016190.1:g.25212_25213delinsAG , LRG_1028:g.25212_25213delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.9894_9895delinsAG MANE Select	ENSP00000357789.1:p.Pro3298=
ENST00000368799.1:c.9894_9895delinsAG	ENSP00000357789.1:p.Pro3298=
NM_002016.1:c.9894_9895delinsAG , LRG_1028t1:c.9894_9895delinsAG	NP_002007.1:p.Pro3298=
XM_011509329.1:c.9108+786_9108+787delinsAG	XP_011507631.1:n.9108+786_9108+787delinsAG
NM_002016.2:c.9894_9895delinsAG MANE Select	NP_002007.1:p.Pro3298=