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UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA342076698
Gene: FLG
HGNC
NCBI
Linked Data
dbSNP Id:
rs112252908
gnomAD v2:
1-152283173-T-A
gnomAD v4:
1-152310697-T-A
MyVariant Identifiers:
chr1:g.152283173T>A (hg19)
chr1:g.152310697T>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.152310697T>A , CM000663.2:g.152310697T>A
GRCh38
NC_000001.10:g.152283173T>A , CM000663.1:g.152283173T>A
GRCh37
NC_000001.9:g.150549797T>A
NCBI36
NG_016190.1:g.19507A>T , LRG_1028:g.19507A>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000368799.2:c.4189A>T
MANE Select
ENSP00000357789.1:p.Asn1397Tyr
ENST00000368799.1:c.4189A>T
ENSP00000357789.1:p.Asn1397Tyr
NM_002016.1:c.4189A>T , LRG_1028t1:c.4189A>T
NP_002007.1:p.Asn1397Tyr
XM_011509329.1:c.4189A>T
XP_011507631.1:p.Asn1397Tyr
NM_002016.2:c.4189A>T
MANE Select
NP_002007.1:p.Asn1397Tyr
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