Canonical Allele Identifier: CA382777892

Gene: SCN4B

Linked Data

• MyVariant Identifiers: chr11:g.118014577G>T (hg19) ; chr11:g.118143862G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118143862G>T , CM000673.2:g.118143862G>T	GRCh38
NC_000011.9:g.118014577G>T , CM000673.1:g.118014577G>T	GRCh37
NC_000011.8:g.117519787G>T	NCBI36
NG_011710.1:g.14054C>A , LRG_330:g.14054C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.434C>A MANE Select	ENSP00000322460.4:p.Ala145Asp
ENST00000324727.8:c.434C>A	ENSP00000322460.4:p.Ala145Asp
ENST00000415030.6:n.577C>A
ENST00000529878.1:c.62-2526C>A	ENSP00000436343.1:n.62-2526C>A
ENST00000532138.1:n.719+125C>A
NM_001142348.1:c.62-2526C>A	NP_001135820.1:n.62-2526C>A
NM_001142349.1:c.104C>A	NP_001135821.1:p.Ala35Asp
NM_174934.3:c.434C>A , LRG_330t1:c.434C>A	NP_777594.1:p.Ala145Asp
NR_024527.1:n.488+125C>A
NM_001142348.2:c.62-2526C>A	NP_001135820.1:n.62-2526C>A
NM_001142349.2:c.104C>A	NP_001135821.1:p.Ala35Asp
NR_024527.2:n.452+125C>A
NM_174934.4:c.434C>A MANE Select	NP_777594.1:p.Ala145Asp