Canonical Allele Identifier: CA382777443

Gene: SCN4B

Linked Data

• MyVariant Identifiers: chr11:g.118011940T>A (hg19) ; chr11:g.118141225T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141225T>A , CM000673.2:g.118141225T>A	GRCh38
NC_000011.9:g.118011940T>A , CM000673.1:g.118011940T>A	GRCh37
NC_000011.8:g.117517150T>A	NCBI36
NG_011710.1:g.16691A>T , LRG_330:g.16691A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.575A>T MANE Select	ENSP00000322460.4:p.Lys192Met
ENST00000324727.8:c.575A>T	ENSP00000322460.4:p.Lys192Met
ENST00000415030.6:n.718A>T
ENST00000423160.2:n.209A>T
ENST00000529878.1:c.173A>T	ENSP00000436343.1:p.Lys58Met
ENST00000531550.1:n.640A>T
ENST00000532138.1:n.831A>T
NM_001142348.1:c.173A>T	NP_001135820.1:p.Lys58Met
NM_001142349.1:c.245A>T	NP_001135821.1:p.Lys82Met
NM_174934.3:c.575A>T , LRG_330t1:c.575A>T	NP_777594.1:p.Lys192Met
NR_024527.1:n.600A>T
NM_001142348.2:c.173A>T	NP_001135820.1:p.Lys58Met
NM_001142349.2:c.245A>T	NP_001135821.1:p.Lys82Met
NR_024527.2:n.564A>T
NM_174934.4:c.575A>T MANE Select	NP_777594.1:p.Lys192Met