Canonical Allele Identifier: CA8708749

Gene: SCN4A

Linked Data

• ClinVar Variation Id: 324505
• ClinVar RCV Id: RCV000278763 ; RCV000301249 ; RCV000336430 ; RCV000404426 ; RCV000408363
• dbSNP Id: rs761023866
• ExAC: 17:62018185 G / A
• gnomAD v2: 17-62018185-G-A
• gnomAD v3: 17-63940825-G-A
• gnomAD v4: 17-63940825-G-A
• MyVariant Identifiers: chr17:g.62018185G>A (hg19) ; chr17:g.63940825G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63940825G>A , CM000679.2:g.63940825G>A	GRCh38
NC_000017.10:g.62018185G>A , CM000679.1:g.62018185G>A	GRCh37
NC_000017.9:g.59371917G>A	NCBI36
NG_011699.1:g.37094C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435607.3:c.5457C>T MANE Select	ENSP00000396320.1:p.Pro1819=
ENST00000578147.5:c.5457C>T	ENSP00000463963.1:p.Pro1819=
NM_000334.4:c.5457C>T MANE Select	NP_000325.4:p.Pro1819=
XM_005257566.3:c.5457C>T	XP_005257623.1:p.Pro1819=