Canonical Allele Identifier: CA2647993593
Gene: FLG HGNC NCBI

Linked Data

gnomAD v4: 1-152310776-GTGTCTGGAGCTGTCTGCTGACTGCTGGTGGCGGGATCCATGTCTTTCTCCTGGACTTGATCTTGCCTGTTCATGGGATGACACAGCCTGTCCATGAGAGGAAGACTCTGTGTGATGAGTGCCTGAT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152310794_152310919del , CM000663.2:g.152310794_152310919del GRCh38
NC_000001.10:g.152283270_152283395del , CM000663.1:g.152283270_152283395del GRCh37
NC_000001.9:g.150549894_150550019del NCBI36
NG_016190.1:g.19302_19427del , LRG_1028:g.19302_19427del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.3984_4109del MANE Select ENSP00000357789.1:p.Gln1328_Arg1369del
ENST00000368799.1:c.3984_4109del ENSP00000357789.1:p.Gln1328_Arg1369del
NM_002016.1:c.3984_4109del , LRG_1028t1:c.3984_4109del NP_002007.1:p.Gln1328_Arg1369del
XM_011509329.1:c.3984_4109del XP_011507631.1:p.Gln1328_Arg1369del
NM_002016.2:c.3984_4109del MANE Select NP_002007.1:p.Gln1328_Arg1369del
Search 100 bp 5'
Search 100 bp 3'