Canonical Allele Identifier: CA2003367889

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141246T= , CM000673.2:g.118141246T=	GRCh38
NC_000011.9:g.118011961T= , CM000673.1:g.118011961T=	GRCh37
NC_000011.8:g.117517171T=	NCBI36
NG_011710.1:g.16670A= , LRG_330:g.16670A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.554A= MANE Select	ENSP00000322460.4:p.Lys185=
ENST00000324727.8:c.554A=	ENSP00000322460.4:p.Lys185=
ENST00000415030.6:n.697A=
ENST00000423160.2:n.188A=
ENST00000529878.1:c.152A=	ENSP00000436343.1:p.Lys51=
ENST00000531550.1:n.619A=
ENST00000532138.1:n.810A=
NM_001142348.1:c.152A=	NP_001135820.1:p.Lys51=
NM_001142349.1:c.224A=	NP_001135821.1:p.Lys75=
NM_174934.3:c.554A= , LRG_330t1:c.554A=	NP_777594.1:p.Lys185=
NR_024527.1:n.579A=
NM_001142348.2:c.152A=	NP_001135820.1:p.Lys51=
NM_001142349.2:c.224A=	NP_001135821.1:p.Lys75=
NR_024527.2:n.543A=
NM_174934.4:c.554A= MANE Select	NP_777594.1:p.Lys185=