Canonical Allele Identifier: CA2003367931

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141323G= , CM000673.2:g.118141323G=	GRCh38
NC_000011.9:g.118012038G= , CM000673.1:g.118012038G=	GRCh37
NC_000011.8:g.117517248G=	NCBI36
NG_011710.1:g.16593C= , LRG_330:g.16593C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324727.9:c.477C= MANE Select	ENSP00000322460.4:p.Asp159=
ENST00000324727.8:c.477C=	ENSP00000322460.4:p.Asp159=
ENST00000415030.6:n.620C=
ENST00000423160.2:n.111C=
ENST00000529878.1:c.75C=	ENSP00000436343.1:p.Asp25=
ENST00000531550.1:n.542C=
ENST00000532138.1:n.733C=
NM_001142348.1:c.75C=	NP_001135820.1:p.Asp25=
NM_001142349.1:c.147C=	NP_001135821.1:p.Asp49=
NM_174934.3:c.477C= , LRG_330t1:c.477C=	NP_777594.1:p.Asp159=
NR_024527.1:n.502C=
NM_001142348.2:c.75C=	NP_001135820.1:p.Asp25=
NM_001142349.2:c.147C=	NP_001135821.1:p.Asp49=
NR_024527.2:n.466C=
NM_174934.4:c.477C= MANE Select	NP_777594.1:p.Asp159=