Canonical Allele Identifier: CA2574993152

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141342_118141343del , CM000673.2:g.118141342_118141343del	GRCh38
NC_000011.9:g.118012057_118012058del , CM000673.1:g.118012057_118012058del	GRCh37
NC_000011.8:g.117517267_117517268del	NCBI36
NG_011710.1:g.16577_16578del , LRG_330:g.16577_16578del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.464-3_464-2del MANE Select	ENSP00000322460.4:n.464-3_464-2del
ENST00000324727.8:c.464-3_464-2del	ENSP00000322460.4:n.464-3_464-2del
ENST00000415030.6:n.607-3_607-2del
ENST00000423160.2:n.98-3_98-2del
ENST00000529878.1:c.62-3_62-2del	ENSP00000436343.1:n.62-3_62-2del
ENST00000531550.1:n.526_527del
ENST00000532138.1:n.720-3_720-2del
NM_001142348.1:c.62-3_62-2del	NP_001135820.1:n.62-3_62-2del
NM_001142349.1:c.134-3_134-2del	NP_001135821.1:n.134-3_134-2del
NM_174934.3:c.464-3_464-2del , LRG_330t1:c.464-3_464-2del	NP_777594.1:n.464-3_464-2del
NR_024527.1:n.489-3_489-2del
NM_001142348.2:c.62-3_62-2del	NP_001135820.1:n.62-3_62-2del
NM_001142349.2:c.134-3_134-2del	NP_001135821.1:n.134-3_134-2del
NR_024527.2:n.453-3_453-2del
NM_174934.4:c.464-3_464-2del MANE Select	NP_777594.1:n.464-3_464-2del