Canonical Allele Identifier: CA2270160814
Gene: SCN4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63941169_63941172delinsACTT , CM000679.2:g.63941169_63941172delinsACTT GRCh38
NC_000017.10:g.62018529_62018532delinsACTT , CM000679.1:g.62018529_62018532delinsACTT GRCh37
NC_000017.9:g.59372261_59372264delinsACTT NCBI36
NG_011699.1:g.36747_36750delinsAAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.5110_5113delinsAAGT MANE Select ENSP00000396320.1:p.Lys1704=
ENST00000578147.5:c.5110_5113delinsAAGT ENSP00000463963.1:p.Lys1704=
NM_000334.4:c.5110_5113delinsAAGT MANE Select NP_000325.4:p.Lys1704=
XM_005257566.3:c.5110_5113delinsAAGT XP_005257623.1:p.Lys1704=