Canonical Allele Identifier: CA2003369001

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118143830T= , CM000673.2:g.118143830T=	GRCh38
NC_000011.9:g.118014545T= , CM000673.1:g.118014545T=	GRCh37
NC_000011.8:g.117519755T=	NCBI36
NG_011710.1:g.14086A= , LRG_330:g.14086A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.463+3A= MANE Select	ENSP00000322460.4:n.463+3A=
ENST00000324727.8:c.463+3A=	ENSP00000322460.4:n.463+3A=
ENST00000415030.6:n.606+3A=
ENST00000529878.1:c.62-2494A=	ENSP00000436343.1:n.62-2494A=
ENST00000532138.1:n.719+157A=
NM_001142348.1:c.62-2494A=	NP_001135820.1:n.62-2494A=
NM_001142349.1:c.133+3A=	NP_001135821.1:n.133+3A=
NM_174934.3:c.463+3A= , LRG_330t1:c.463+3A=	NP_777594.1:n.463+3A=
NR_024527.1:n.488+157A=
NM_001142348.2:c.62-2494A=	NP_001135820.1:n.62-2494A=
NM_001142349.2:c.133+3A=	NP_001135821.1:n.133+3A=
NR_024527.2:n.452+157A=
NM_174934.4:c.463+3A= MANE Select	NP_777594.1:n.463+3A=