Canonical Allele Identifier: CA2479953346
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152315276_152315280delinsGAAAA , CM000663.2:g.152315276_152315280delinsGAAAA GRCh38
NC_000001.10:g.152287752_152287756delinsGAAAA , CM000663.1:g.152287752_152287756delinsGAAAA GRCh37
NC_000001.9:g.150554376_150554380delinsGAAAA NCBI36
NG_016190.1:g.14924_14928delinsTTTTC , LRG_1028:g.14924_14928delinsTTTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.138+39_138+43delinsTTTTC MANE Select ENSP00000357789.1:n.138+39_138+43delinsTTTTC
ENST00000368799.1:c.138+39_138+43delinsTTTTC ENSP00000357789.1:n.138+39_138+43delinsTTTTC
NM_002016.1:c.138+39_138+43delinsTTTTC , LRG_1028t1:c.138+39_138+43delinsTTTTC NP_002007.1:n.138+39_138+43delinsTTTTC
NR_103778.1:n.914+319_914+323delinsGAAAA
XM_011509329.1:c.138+39_138+43delinsTTTTC XP_011507631.1:n.138+39_138+43delinsTTTTC
NM_002016.2:c.138+39_138+43delinsTTTTC MANE Select NP_002007.1:n.138+39_138+43delinsTTTTC