Canonical Allele Identifier: CA420931963

Gene: FLG

Linked Data

• MyVariant Identifiers: chr1:g.152286375T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152313899T>G , CM000663.2:g.152313899T>G	GRCh38
NC_000001.10:g.152286375T>G , CM000663.1:g.152286375T>G	GRCh37
NC_000001.9:g.150552999T>G	NCBI36
NG_016190.1:g.16305A>C , LRG_1028:g.16305A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000368799.2:c.987A>C MANE Select	ENSP00000357789.1:p.Ser329=
ENST00000368799.1:c.987A>C	ENSP00000357789.1:p.Ser329=
NM_002016.1:c.987A>C , LRG_1028t1:c.987A>C	NP_002007.1:p.Ser329=
NR_103778.1:n.441T>G
XM_011509329.1:c.987A>C	XP_011507631.1:p.Ser329=
NM_002016.2:c.987A>C MANE Select	NP_002007.1:p.Ser329=