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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:
CA341679
Gene: SCN4A
HGNC
NCBI
Linked Data
dbSNP Id:
rs80338961
MyVariant Identifiers:
chr17:g.62019159T>A (hg19)
chr17:g.63941799T>A (hg38)
PubMed:
PMID:11971097
PMID:20301669
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.63941799T>A , CM000679.2:g.63941799T>A
GRCh38
NC_000017.10:g.62019159T>A , CM000679.1:g.62019159T>A
GRCh37
NC_000017.9:g.59372891T>A
NCBI36
NG_011699.1:g.36120A>T
Transcript Alleles
HGVS
Amino-acid change
ENST00000435607.3:c.4483A>T
MANE Select
ENSP00000396320.1:p.Ile1495Phe
ENST00000578147.5:c.4483A>T
ENSP00000463963.1:p.Ile1495Phe
NM_000334.4:c.4483A>T
MANE Select
NP_000325.4:p.Ile1495Phe
XM_005257566.3:c.4483A>T
XP_005257623.1:p.Ile1495Phe
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