Canonical Allele Identifier: CA2270162583
Gene: SCN4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63944631_63944632delinsGC , CM000679.2:g.63944631_63944632delinsGC GRCh38
NC_000017.10:g.62021991_62021992delinsGC , CM000679.1:g.62021991_62021992delinsGC GRCh37
NC_000017.9:g.59375723_59375724delinsGC NCBI36
NG_011699.1:g.33287_33288delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.3912+41_3912+42delinsGC MANE Select ENSP00000396320.1:n.3912+41_3912+42delins...
ENST00000578147.5:c.3916+37_3916+38delinsGC ENSP00000463963.1:n.3916+37_3916+38delins...
NM_000334.4:c.3912+41_3912+42delinsGC MANE Select NP_000325.4:n.3912+41_3912+42delinsGC
XM_005257566.3:c.3912+41_3912+42delinsGC XP_005257623.1:n.3912+41_3912+42delinsGC