Canonical Allele Identifier: CA342083285
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095474
ClinVar RCV Id: RCV004386792
MyVariant Identifiers: chr1:g.152283916G>A (hg19) chr1:g.152311440G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311440G>A , CM000663.2:g.152311440G>A GRCh38
NC_000001.10:g.152283916G>A , CM000663.1:g.152283916G>A GRCh37
NC_000001.9:g.150550540G>A NCBI36
NG_016190.1:g.18764C>T , LRG_1028:g.18764C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.3446C>T MANE Select ENSP00000357789.1:p.Ala1149Val
ENST00000368799.1:c.3446C>T ENSP00000357789.1:p.Ala1149Val
NM_002016.1:c.3446C>T , LRG_1028t1:c.3446C>T NP_002007.1:p.Ala1149Val
XM_011509329.1:c.3446C>T XP_011507631.1:p.Ala1149Val
NM_002016.2:c.3446C>T MANE Select NP_002007.1:p.Ala1149Val
Search 100 bp 5'
Search 100 bp 3'