Canonical Allele Identifier: CA1106648
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs754087511
ExAC: 1:152283856 G / T
gnomAD v2: 1-152283856-G-T
gnomAD v4: 1-152311380-G-T
COSMIC: COSM1743363
MyVariant Identifiers: chr1:g.152283856G>T (hg19) chr1:g.152311380G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311380G>T , CM000663.2:g.152311380G>T GRCh38
NC_000001.10:g.152283856G>T , CM000663.1:g.152283856G>T GRCh37
NC_000001.9:g.150550480G>T NCBI36
NG_016190.1:g.18824C>A , LRG_1028:g.18824C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.3506C>A MANE Select ENSP00000357789.1:p.Pro1169Gln
ENST00000368799.1:c.3506C>A ENSP00000357789.1:p.Pro1169Gln
NM_002016.1:c.3506C>A , LRG_1028t1:c.3506C>A NP_002007.1:p.Pro1169Gln
XM_011509329.1:c.3506C>A XP_011507631.1:p.Pro1169Gln
NM_002016.2:c.3506C>A MANE Select NP_002007.1:p.Pro1169Gln
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