Canonical Allele Identifier: CA342061539
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs541394374

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152309148T>G , CM000663.2:g.152309148T>G GRCh38
NC_000001.10:g.152281624T>G , CM000663.1:g.152281624T>G GRCh37
NC_000001.9:g.150548248T>G NCBI36
NG_016190.1:g.21056A>C , LRG_1028:g.21056A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5738A>C MANE Select ENSP00000357789.1:p.Asn1913Thr
ENST00000368799.1:c.5738A>C ENSP00000357789.1:p.Asn1913Thr
NM_002016.1:c.5738A>C , LRG_1028t1:c.5738A>C NP_002007.1:p.Asn1913Thr
XM_011509329.1:c.5738A>C XP_011507631.1:p.Asn1913Thr
NM_002016.2:c.5738A>C MANE Select NP_002007.1:p.Asn1913Thr