Canonical Allele Identifier: CA2616226155

Gene: SCN4B

Linked Data

• gnomAD v4: 11-118141393-GGAGCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141397_118141401del , CM000673.2:g.118141397_118141401del	GRCh38
NC_000011.9:g.118012112_118012116del , CM000673.1:g.118012112_118012116del	GRCh37
NC_000011.8:g.117517322_117517326del	NCBI36
NG_011710.1:g.16518_16522del , LRG_330:g.16518_16522del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.464-62_464-58del MANE Select	ENSP00000322460.4:n.464-62_464-58del
ENST00000324727.8:c.464-62_464-58del	ENSP00000322460.4:n.464-62_464-58del
ENST00000415030.6:n.607-62_607-58del
ENST00000423160.2:n.98-62_98-58del
ENST00000529878.1:c.62-62_62-58del	ENSP00000436343.1:n.62-62_62-58del
ENST00000531550.1:n.467_471del
ENST00000532138.1:n.720-62_720-58del
NM_001142348.1:c.62-62_62-58del	NP_001135820.1:n.62-62_62-58del
NM_001142349.1:c.134-62_134-58del	NP_001135821.1:n.134-62_134-58del
NM_174934.3:c.464-62_464-58del , LRG_330t1:c.464-62_464-58del	NP_777594.1:n.464-62_464-58del
NR_024527.1:n.489-62_489-58del
NM_001142348.2:c.62-62_62-58del	NP_001135820.1:n.62-62_62-58del
NM_001142349.2:c.134-62_134-58del	NP_001135821.1:n.134-62_134-58del
NR_024527.2:n.453-62_453-58del
NM_174934.4:c.464-62_464-58del MANE Select	NP_777594.1:n.464-62_464-58del