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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:
CA16620554
Gene: SCN4A
HGNC
NCBI
Linked Data
ClinVar Variation Id:
421864
ClinVar RCV Id:
RCV000484396
RCV001061560
dbSNP Id:
rs1064795409
MyVariant Identifiers:
chr17:g.62019215A>G (hg19)
chr17:g.63941855A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.63941855A>G , CM000679.2:g.63941855A>G
GRCh38
NC_000017.10:g.62019215A>G , CM000679.1:g.62019215A>G
GRCh37
NC_000017.9:g.59372947A>G
NCBI36
NG_011699.1:g.36064T>C
Transcript Alleles
HGVS
Amino-acid change
ENST00000435607.3:c.4427T>C
MANE Select
ENSP00000396320.1:p.Met1476Thr
ENST00000578147.5:c.4427T>C
ENSP00000463963.1:p.Met1476Thr
NM_000334.4:c.4427T>C
MANE Select
NP_000325.4:p.Met1476Thr
XM_005257566.3:c.4427T>C
XP_005257623.1:p.Met1476Thr
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