Canonical Allele Identifier: CA384904492

Gene: SCN8A

Linked Data

• MyVariant Identifiers: chr12:g.52180356C>A (hg19) ; chr12:g.51786572C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51786572C>A , CM000674.2:g.51786572C>A	GRCh38
NC_000012.11:g.52180356C>A , CM000674.1:g.52180356C>A	GRCh37
NC_000012.10:g.50466623C>A	NCBI36
NG_021180.2:g.200337C>A
NG_021180.3:g.201615C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354534.11:c.3973C>A MANE Plus Clinical	ENSP00000346534.4:p.Pro1325Thr
ENST00000548086.3:c.1767C>A
ENST00000627620.5:c.3973C>A MANE Select	ENSP00000487583.2:p.Pro1325Thr
ENST00000636945.2:c.2037C>A
ENST00000662684.1:c.3973C>A	ENSP00000499636.1:p.Pro1325Thr
ENST00000668547.1:c.3850C>A	ENSP00000499691.1:p.Pro1284Thr
ENST00000354534.10:c.3973C>A	ENSP00000346534.4:p.Pro1325Thr
ENST00000355133.7:c.3850C>A	ENSP00000347255.4:p.Pro1284Thr
ENST00000545061.5:c.3850C>A	ENSP00000440360.1:p.Pro1284Thr
ENST00000548086.1:n.224C>A
ENST00000599343.5:c.4006C>A	ENSP00000476447.3:p.Pro1336Thr
ENST00000627620.2:c.3973C>A	ENSP00000487583.1:p.Pro1325Thr
NM_001177984.2:c.3850C>A	NP_001171455.1:p.Pro1284Thr
NM_014191.3:c.3973C>A	NP_055006.1:p.Pro1325Thr
XM_006719556.2:c.3973C>A	XP_006719619.1:p.Pro1325Thr
XM_011538650.1:c.3973C>A	XP_011536952.1:p.Pro1325Thr
XM_011538651.1:c.3973C>A	XP_011536953.1:p.Pro1325Thr
NM_001330260.1:c.3973C>A	NP_001317189.1:p.Pro1325Thr
XM_006719556.4:c.3973C>A	XP_006719619.1:p.Pro1325Thr
XM_011538651.3:c.3973C>A	XP_011536953.1:p.Pro1325Thr
XM_017019794.2:c.3973C>A	XP_016875283.1:p.Pro1325Thr
XM_017019795.2:c.3850C>A	XP_016875284.1:p.Pro1284Thr
XM_017019796.1:c.*71C>A	XP_016875285.1:n.*71C>A
NM_001330260.2:c.3973C>A MANE Select	NP_001317189.1:p.Pro1325Thr
NM_001369788.1:c.3850C>A	NP_001356717.1:p.Pro1284Thr
NM_014191.4:c.3973C>A MANE Plus Clinical	NP_055006.1:p.Pro1325Thr
NM_001177984.3:c.3850C>A	NP_001171455.1:p.Pro1284Thr