Canonical Allele Identifier: CA2003367899

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141265G= , CM000673.2:g.118141265G=	GRCh38
NC_000011.9:g.118011980G= , CM000673.1:g.118011980G=	GRCh37
NC_000011.8:g.117517190G=	NCBI36
NG_011710.1:g.16651C= , LRG_330:g.16651C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.535C= MANE Select	ENSP00000322460.4:p.Leu179=
ENST00000324727.8:c.535C=	ENSP00000322460.4:p.Leu179=
ENST00000415030.6:n.678C=
ENST00000423160.2:n.169C=
ENST00000529878.1:c.133C=	ENSP00000436343.1:p.Leu45=
ENST00000531550.1:n.600C=
ENST00000532138.1:n.791C=
NM_001142348.1:c.133C=	NP_001135820.1:p.Leu45=
NM_001142349.1:c.205C=	NP_001135821.1:p.Leu69=
NM_174934.3:c.535C= , LRG_330t1:c.535C=	NP_777594.1:p.Leu179=
NR_024527.1:n.560C=
NM_001142348.2:c.133C=	NP_001135820.1:p.Leu45=
NM_001142349.2:c.205C=	NP_001135821.1:p.Leu69=
NR_024527.2:n.524C=
NM_174934.4:c.535C= MANE Select	NP_777594.1:p.Leu179=