Canonical Allele Identifier: CA400618302
Gene: SCN4A HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.62022918G>T (hg19) chr17:g.63945558G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63945558G>T , CM000679.2:g.63945558G>T GRCh38
NC_000017.10:g.62022918G>T , CM000679.1:g.62022918G>T GRCh37
NC_000017.9:g.59376650G>T NCBI36
NG_011699.1:g.32361C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.3522C>A MANE Select ENSP00000396320.1:p.Phe1174Leu
ENST00000578147.5:c.3522C>A ENSP00000463963.1:p.Phe1174Leu
NM_000334.4:c.3522C>A MANE Select NP_000325.4:p.Phe1174Leu
XM_005257566.3:c.3522C>A XP_005257623.1:p.Phe1174Leu
Search 100 bp 5'
Search 100 bp 3'