Canonical Allele Identifier: CA400614574

Gene: SCN4A

Linked Data

• dbSNP Id: rs1359548805
• gnomAD v2: 17-62018739-T-C
• gnomAD v4: 17-63941379-T-C
• MyVariant Identifiers: chr17:g.62018739T>C (hg19) ; chr17:g.63941379T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63941379T>C , CM000679.2:g.63941379T>C	GRCh38
NC_000017.10:g.62018739T>C , CM000679.1:g.62018739T>C	GRCh37
NC_000017.9:g.59372471T>C	NCBI36
NG_011699.1:g.36540A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435607.3:c.4903A>G MANE Select	ENSP00000396320.1:p.Ile1635Val
ENST00000578147.5:c.4903A>G	ENSP00000463963.1:p.Ile1635Val
NM_000334.4:c.4903A>G MANE Select	NP_000325.4:p.Ile1635Val
XM_005257566.3:c.4903A>G	XP_005257623.1:p.Ile1635Val