Canonical Allele Identifier: CA2479949438
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152308011_152308012delinsTG , CM000663.2:g.152308011_152308012delinsTG GRCh38
NC_000001.10:g.152280487_152280488delinsTG , CM000663.1:g.152280487_152280488delinsTG GRCh37
NC_000001.9:g.150547111_150547112delinsTG NCBI36
NG_016190.1:g.22192_22193delinsCA , LRG_1028:g.22192_22193delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.6874_6875delinsCA MANE Select ENSP00000357789.1:p.His2292=
ENST00000368799.1:c.6874_6875delinsCA ENSP00000357789.1:p.His2292=
NM_002016.1:c.6874_6875delinsCA , LRG_1028t1:c.6874_6875delinsCA NP_002007.1:p.His2292=
XM_011509329.1:c.6874_6875delinsCA XP_011507631.1:p.His2292=
NM_002016.2:c.6874_6875delinsCA MANE Select NP_002007.1:p.His2292=