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ClinGen Allele Registry
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Canonical Allele Identifier:
CA501348599
Community Standard Title: NM_000334.4(SCN4A):c.3696G>A (p.Leu1232=)
Gene: SCN4A
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.63945384C>T , CM000679.2:g.63945384C>T
GRCh38
NC_000017.10:g.62022744C>T , CM000679.1:g.62022744C>T
GRCh37
NC_000017.9:g.59376476C>T
NCBI36
NG_011699.1:g.32535G>A
Transcript Alleles
HGVS
Amino-acid Change
NM_000334.4:c.3696G>A
MANE Select
NP_000325.4:p.Leu1232=
ENST00000435607.3:c.3696G>A
MANE Select
ENSP00000396320.1:p.Leu1232=
ENST00000578147.5:c.3696G>A
ENSP00000463963.1:p.Leu1232=
XM_005257566.3:c.3696G>A
XP_005257623.1:p.Leu1232=
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