Canonical Allele Identifier: CA645527651
Gene: FLG HGNC NCBI

Linked Data

COSMIC: COSM6121286
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152307642_152307643delinsTT , CM000663.2:g.152307642_152307643delinsTT GRCh38
NC_000001.10:g.152280118_152280119delinsTT , CM000663.1:g.152280118_152280119delinsTT GRCh37
NC_000001.9:g.150546742_150546743delinsTT NCBI36
NG_016190.1:g.22561_22562delinsAA , LRG_1028:g.22561_22562delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.7243_7244delinsAA MANE Select ENSP00000357789.1:p.Leu2415Asn
ENST00000368799.1:c.7243_7244delinsAA ENSP00000357789.1:p.Leu2415Asn
NM_002016.1:c.7243_7244delinsAA , LRG_1028t1:c.7243_7244delinsAA NP_002007.1:p.Leu2415Asn
XM_011509329.1:c.7243_7244delinsAA XP_011507631.1:p.Leu2415Asn
NM_002016.2:c.7243_7244delinsAA MANE Select NP_002007.1:p.Leu2415Asn
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