Canonical Allele Identifier: CA400614009
Gene: SCN4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63941170C>G , CM000679.2:g.63941170C>G GRCh38
NC_000017.10:g.62018530C>G , CM000679.1:g.62018530C>G GRCh37
NC_000017.9:g.59372262C>G NCBI36
NG_011699.1:g.36749G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.5112G>C MANE Select ENSP00000396320.1:p.Lys1704Asn
ENST00000578147.5:c.5112G>C ENSP00000463963.1:p.Lys1704Asn
NM_000334.4:c.5112G>C MANE Select NP_000325.4:p.Lys1704Asn
XM_005257566.3:c.5112G>C XP_005257623.1:p.Lys1704Asn