Canonical Allele Identifier: CA420926666

Gene: FLG

Linked Data

• MyVariant Identifiers: chr1:g.152277141A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304665A>C , CM000663.2:g.152304665A>C	GRCh38
NC_000001.10:g.152277141A>C , CM000663.1:g.152277141A>C	GRCh37
NC_000001.9:g.150543765A>C	NCBI36
NG_016190.1:g.25539T>G , LRG_1028:g.25539T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000368799.2:c.10221T>G MANE Select	ENSP00000357789.1:p.Thr3407=
ENST00000368799.1:c.10221T>G	ENSP00000357789.1:p.Thr3407=
NM_002016.1:c.10221T>G , LRG_1028t1:c.10221T>G	NP_002007.1:p.Thr3407=
XM_011509329.1:c.9109-832T>G	XP_011507631.1:n.9109-832T>G
NM_002016.2:c.10221T>G MANE Select	NP_002007.1:p.Thr3407=