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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:
CA292966944
Gene: SCN4A
HGNC
NCBI
Linked Data
ClinVar Variation Id:
843445
ClinVar RCV Id:
RCV001046074
dbSNP Id:
rs897448432
gnomAD v2:
17-62036639-G-A
gnomAD v4:
17-63959279-G-A
MyVariant Identifiers:
chr17:g.62036639G>A (hg19)
chr17:g.63959279G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.63959279G>A , CM000679.2:g.63959279G>A
GRCh38
NC_000017.10:g.62036639G>A , CM000679.1:g.62036639G>A
GRCh37
NC_000017.9:g.59390371G>A
NCBI36
NG_011699.1:g.18640C>T
Transcript Alleles
HGVS
Amino-acid change
ENST00000435607.3:c.2005C>T
MANE Select
ENSP00000396320.1:p.Arg669Cys
ENST00000578147.5:c.2005C>T
ENSP00000463963.1:p.Arg669Cys
NM_000334.4:c.2005C>T
MANE Select
NP_000325.4:p.Arg669Cys
XM_005257566.3:c.2005C>T
XP_005257623.1:p.Arg669Cys
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