Canonical Allele Identifier: CA2639309767
Gene: SCN4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63944634C>A , CM000679.2:g.63944634C>A GRCh38
NC_000017.10:g.62021994C>A , CM000679.1:g.62021994C>A GRCh37
NC_000017.9:g.59375726C>A NCBI36
NG_011699.1:g.33285G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.3912+39G>T MANE Select ENSP00000396320.1:n.3912+39G>T
ENST00000578147.5:c.3916+35G>T ENSP00000463963.1:n.3916+35G>T
NM_000334.4:c.3912+39G>T MANE Select NP_000325.4:n.3912+39G>T
XM_005257566.3:c.3912+39G>T XP_005257623.1:n.3912+39G>T