Canonical Allele Identifier: CA501348641
Gene: SCN4A HGNC NCBI

Linked Data

dbSNP Id: rs1908684537
gnomAD v3: 17-63945444-G-A
gnomAD v4: 17-63945444-G-A
MyVariant Identifiers: chr17:g.62022804G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63945444G>A , CM000679.2:g.63945444G>A GRCh38
NC_000017.10:g.62022804G>A , CM000679.1:g.62022804G>A GRCh37
NC_000017.9:g.59376536G>A NCBI36
NG_011699.1:g.32475C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.3636C>T MANE Select ENSP00000396320.1:p.Leu1212=
ENST00000578147.5:c.3636C>T ENSP00000463963.1:p.Leu1212=
NM_000334.4:c.3636C>T MANE Select NP_000325.4:p.Leu1212=
XM_005257566.3:c.3636C>T XP_005257623.1:p.Leu1212=
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