Canonical Allele Identifier: CA352175216

Gene: SCN11A

Linked Data

• MyVariant Identifiers: chr3:g.38936454A>T (hg19) ; chr3:g.38894963A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38894963A>T , CM000665.2:g.38894963A>T	GRCh38
NC_000003.11:g.38936454A>T , CM000665.1:g.38936454A>T	GRCh37
NC_000003.10:g.38911458A>T	NCBI36
NG_033859.1:g.60599T>A
NG_033859.2:g.162024T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302328.9:c.2405T>A MANE Select	ENSP00000307599.3:p.Val802Glu
ENST00000668754.1:c.2405T>A	ENSP00000499569.1:p.Val802Glu
ENST00000675223.1:c.2405T>A	ENSP00000502481.1:p.Val802Glu
ENST00000675672.1:c.2405T>A	ENSP00000502446.1:p.Val802Glu
ENST00000675892.1:c.2225T>A	ENSP00000502318.1:p.Val742Glu
ENST00000676045.1:c.2449T>A	ENSP00000501685.1:n.2449T>A
ENST00000676176.1:c.2024T>A	ENSP00000501891.1:p.Val675Glu
ENST00000302328.7:c.2405T>A	ENSP00000307599.3:p.Val802Glu
ENST00000444237.2:c.2405T>A	ENSP00000408028.2:p.Val802Glu
ENST00000456224.7:c.2405T>A	ENSP00000416757.3:p.Val802Glu
NM_001287223.1:c.2405T>A	NP_001274152.1:p.Val802Glu
NM_014139.2:c.2405T>A	NP_054858.2:p.Val802Glu
XM_011533320.1:c.2405T>A	XP_011531622.1:p.Val802Glu
XM_011533321.1:c.1742T>A	XP_011531623.1:p.Val581Glu
XM_011533322.1:c.953T>A	XP_011531624.1:p.Val318Glu
NM_001349253.1:c.2405T>A	NP_001336182.1:p.Val802Glu
XM_011533321.2:c.1742T>A	XP_011531623.1:p.Val581Glu
XM_017005647.1:c.2780T>A	XP_016861136.1:p.Val927Glu
XM_017005648.1:c.2207T>A	XP_016861137.1:p.Val736Glu
XM_017005650.1:c.2405T>A	XP_016861139.1:p.Val802Glu
XM_017005651.1:c.2132T>A	XP_016861140.1:p.Val711Glu
XM_017005652.1:c.2405T>A	XP_016861141.1:p.Val802Glu
XM_017005653.1:c.809T>A	XP_016861142.1:p.Val270Glu
NM_001349253.2:c.2405T>A MANE Select	NP_001336182.1:p.Val802Glu
NM_014139.3:c.2405T>A	NP_054858.2:p.Val802Glu