Canonical Allele Identifier: CA2479949799
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152308683_152308684delinsTG , CM000663.2:g.152308683_152308684delinsTG GRCh38
NC_000001.10:g.152281159_152281160delinsTG , CM000663.1:g.152281159_152281160delinsTG GRCh37
NC_000001.9:g.150547783_150547784delinsTG NCBI36
NG_016190.1:g.21520_21521delinsCA , LRG_1028:g.21520_21521delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.6202_6203delinsCA MANE Select ENSP00000357789.1:p.His2068=
ENST00000368799.1:c.6202_6203delinsCA ENSP00000357789.1:p.His2068=
NM_002016.1:c.6202_6203delinsCA , LRG_1028t1:c.6202_6203delinsCA NP_002007.1:p.His2068=
XM_011509329.1:c.6202_6203delinsCA XP_011507631.1:p.His2068=
NM_002016.2:c.6202_6203delinsCA MANE Select NP_002007.1:p.His2068=