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ClinGen Allele Registry
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Canonical Allele Identifier:
CA8709036
Community Standard Title: NM_000334.4(SCN4A):c.4218C>G (p.Ala1406=)
Gene: SCN4A
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.63942896G>C , CM000679.2:g.63942896G>C
GRCh38
NC_000017.10:g.62020256G>C , CM000679.1:g.62020256G>C
GRCh37
NC_000017.9:g.59373988G>C
NCBI36
NG_011699.1:g.35023C>G
Transcript Alleles
HGVS
Amino-acid Change
NM_000334.4:c.4218C>G
MANE Select
NP_000325.4:p.Ala1406=
ENST00000435607.3:c.4218C>G
MANE Select
ENSP00000396320.1:p.Ala1406=
ENST00000578147.5:c.4218C>G
ENSP00000463963.1:p.Ala1406=
XM_005257566.3:c.4218C>G
XP_005257623.1:p.Ala1406=
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