Canonical Allele Identifier: CA645537916
Gene: FLG HGNC NCBI

Linked Data

COSMIC: COSM344825
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152305073_152305074delinsTC , CM000663.2:g.152305073_152305074delinsTC GRCh38
NC_000001.10:g.152277549_152277550delinsTC , CM000663.1:g.152277549_152277550delinsTC GRCh37
NC_000001.9:g.150544173_150544174delinsTC NCBI36
NG_016190.1:g.25130_25131delinsGA , LRG_1028:g.25130_25131delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9812_9813delinsGA MANE Select ENSP00000357789.1:p.Ser3271Ter
ENST00000368799.1:c.9812_9813delinsGA ENSP00000357789.1:p.Ser3271Ter
NM_002016.1:c.9812_9813delinsGA , LRG_1028t1:c.9812_9813delinsGA NP_002007.1:p.Ser3271Ter
XM_011509329.1:c.9108+704_9108+705delinsGA XP_011507631.1:n.9108+704_9108+705delinsGA
NM_002016.2:c.9812_9813delinsGA MANE Select NP_002007.1:p.Ser3271Ter
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