Canonical Allele Identifier: CA2003367881

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141222T= , CM000673.2:g.118141222T=	GRCh38
NC_000011.9:g.118011937T= , CM000673.1:g.118011937T=	GRCh37
NC_000011.8:g.117517147T=	NCBI36
NG_011710.1:g.16694A= , LRG_330:g.16694A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.578A= MANE Select	ENSP00000322460.4:p.Lys193=
ENST00000324727.8:c.578A=	ENSP00000322460.4:p.Lys193=
ENST00000415030.6:n.721A=
ENST00000423160.2:n.212A=
ENST00000529878.1:c.176A=	ENSP00000436343.1:p.Lys59=
ENST00000531550.1:n.643A=
ENST00000532138.1:n.834A=
NM_001142348.1:c.176A=	NP_001135820.1:p.Lys59=
NM_001142349.1:c.248A=	NP_001135821.1:p.Lys83=
NM_174934.3:c.578A= , LRG_330t1:c.578A=	NP_777594.1:p.Lys193=
NR_024527.1:n.603A=
NM_001142348.2:c.176A=	NP_001135820.1:p.Lys59=
NM_001142349.2:c.248A=	NP_001135821.1:p.Lys83=
NR_024527.2:n.567A=
NM_174934.4:c.578A= MANE Select	NP_777594.1:p.Lys193=