Canonical Allele Identifier: CA480061332

Gene: SCN8A

Linked Data

• MyVariant Identifiers: chr12:g.52159565T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51765781T>C , CM000674.2:g.51765781T>C	GRCh38
NC_000012.11:g.52159565T>C , CM000674.1:g.52159565T>C	GRCh37
NC_000012.10:g.50445832T>C	NCBI36
NG_021180.2:g.179546T>C
NG_021180.3:g.180824T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000354534.11:c.2655T>C MANE Plus Clinical	ENSP00000346534.4:p.Ile885=
ENST00000548086.3:c.502T>C
ENST00000627620.5:c.2655T>C MANE Select	ENSP00000487583.2:p.Ile885=
ENST00000636945.2:c.659T>C
ENST00000662684.1:c.2655T>C	ENSP00000499636.1:p.Ile885=
ENST00000668547.1:c.2655T>C	ENSP00000499691.1:p.Ile885=
ENST00000354534.10:c.2655T>C	ENSP00000346534.4:p.Ile885=
ENST00000355133.7:c.2655T>C	ENSP00000347255.4:p.Ile885=
ENST00000545061.5:c.2655T>C	ENSP00000440360.1:p.Ile885=
ENST00000550891.4:n.2783T>C
ENST00000599343.5:c.2688T>C	ENSP00000476447.3:p.Ile896=
ENST00000627620.2:c.2655T>C	ENSP00000487583.1:p.Ile885=
NM_001177984.2:c.2655T>C	NP_001171455.1:p.Ile885=
NM_014191.3:c.2655T>C	NP_055006.1:p.Ile885=
XM_006719556.2:c.2655T>C	XP_006719619.1:p.Ile885=
XM_011538650.1:c.2655T>C	XP_011536952.1:p.Ile885=
XM_011538651.1:c.2655T>C	XP_011536953.1:p.Ile885=
NM_001330260.1:c.2655T>C	NP_001317189.1:p.Ile885=
XM_006719556.4:c.2655T>C	XP_006719619.1:p.Ile885=
XM_011538651.3:c.2655T>C	XP_011536953.1:p.Ile885=
XM_017019794.2:c.2655T>C	XP_016875283.1:p.Ile885=
XM_017019795.2:c.2655T>C	XP_016875284.1:p.Ile885=
XM_017019796.1:c.2655T>C	XP_016875285.1:p.Ile885=
NM_001330260.2:c.2655T>C MANE Select	NP_001317189.1:p.Ile885=
NM_001369788.1:c.2655T>C	NP_001356717.1:p.Ile885=
NM_014191.4:c.2655T>C MANE Plus Clinical	NP_055006.1:p.Ile885=
NM_001177984.3:c.2655T>C	NP_001171455.1:p.Ile885=