Canonical Allele Identifier: CA352175182

Gene: SCN11A

Linked Data

• MyVariant Identifiers: chr3:g.38936438A>C (hg19) ; chr3:g.38894947A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38894947A>C , CM000665.2:g.38894947A>C	GRCh38
NC_000003.11:g.38936438A>C , CM000665.1:g.38936438A>C	GRCh37
NC_000003.10:g.38911442A>C	NCBI36
NG_033859.1:g.60615T>G
NG_033859.2:g.162040T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000302328.9:c.2421T>G MANE Select	ENSP00000307599.3:p.Ile807Met
ENST00000668754.1:c.2421T>G	ENSP00000499569.1:p.Ile807Met
ENST00000675223.1:c.2421T>G	ENSP00000502481.1:p.Ile807Met
ENST00000675672.1:c.2421T>G	ENSP00000502446.1:p.Ile807Met
ENST00000675892.1:c.2241T>G	ENSP00000502318.1:p.Ile747Met
ENST00000676045.1:c.2465T>G	ENSP00000501685.1:n.2465T>G
ENST00000676176.1:c.2040T>G	ENSP00000501891.1:p.Ile680Met
ENST00000302328.7:c.2421T>G	ENSP00000307599.3:p.Ile807Met
ENST00000444237.2:c.2421T>G	ENSP00000408028.2:p.Ile807Met
ENST00000456224.7:c.2421T>G	ENSP00000416757.3:p.Ile807Met
NM_001287223.1:c.2421T>G	NP_001274152.1:p.Ile807Met
NM_014139.2:c.2421T>G	NP_054858.2:p.Ile807Met
XM_011533320.1:c.2421T>G	XP_011531622.1:p.Ile807Met
XM_011533321.1:c.1758T>G	XP_011531623.1:p.Ile586Met
XM_011533322.1:c.969T>G	XP_011531624.1:p.Ile323Met
NM_001349253.1:c.2421T>G	NP_001336182.1:p.Ile807Met
XM_011533321.2:c.1758T>G	XP_011531623.1:p.Ile586Met
XM_017005647.1:c.2796T>G	XP_016861136.1:p.Ile932Met
XM_017005648.1:c.2223T>G	XP_016861137.1:p.Ile741Met
XM_017005650.1:c.2421T>G	XP_016861139.1:p.Ile807Met
XM_017005651.1:c.2148T>G	XP_016861140.1:p.Ile716Met
XM_017005652.1:c.2421T>G	XP_016861141.1:p.Ile807Met
XM_017005653.1:c.825T>G	XP_016861142.1:p.Ile275Met
NM_001349253.2:c.2421T>G MANE Select	NP_001336182.1:p.Ile807Met
NM_014139.3:c.2421T>G	NP_054858.2:p.Ile807Met