Canonical Allele Identifier: CA352174764

Gene: SCN11A

Linked Data

• dbSNP Id: rs2126116178
• gnomAD v4: 3-38894760-C-T
• MyVariant Identifiers: chr3:g.38936251C>T (hg19) ; chr3:g.38894760C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38894760C>T , CM000665.2:g.38894760C>T	GRCh38
NC_000003.11:g.38936251C>T , CM000665.1:g.38936251C>T	GRCh37
NC_000003.10:g.38911255C>T	NCBI36
NG_033859.1:g.60802G>A
NG_033859.2:g.162227G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302328.9:c.2608G>A MANE Select	ENSP00000307599.3:p.Ala870Thr
ENST00000668754.1:c.2608G>A	ENSP00000499569.1:p.Ala870Thr
ENST00000675223.1:c.2608G>A	ENSP00000502481.1:p.Ala870Thr
ENST00000675672.1:c.2608G>A	ENSP00000502446.1:p.Ala870Thr
ENST00000675892.1:c.2428G>A	ENSP00000502318.1:p.Ala810Thr
ENST00000676045.1:c.2652G>A	ENSP00000501685.1:n.2652G>A
ENST00000676176.1:c.2227G>A	ENSP00000501891.1:p.Ala743Thr
ENST00000302328.7:c.2608G>A	ENSP00000307599.3:p.Ala870Thr
ENST00000444237.2:c.2608G>A	ENSP00000408028.2:p.Ala870Thr
ENST00000456224.7:c.2608G>A	ENSP00000416757.3:p.Ala870Thr
NM_001287223.1:c.2608G>A	NP_001274152.1:p.Ala870Thr
NM_014139.2:c.2608G>A	NP_054858.2:p.Ala870Thr
XM_011533320.1:c.2608G>A	XP_011531622.1:p.Ala870Thr
XM_011533321.1:c.1945G>A	XP_011531623.1:p.Ala649Thr
XM_011533322.1:c.1156G>A	XP_011531624.1:p.Ala386Thr
NM_001349253.1:c.2608G>A	NP_001336182.1:p.Ala870Thr
XM_011533321.2:c.1945G>A	XP_011531623.1:p.Ala649Thr
XM_017005647.1:c.2983G>A	XP_016861136.1:p.Ala995Thr
XM_017005648.1:c.2410G>A	XP_016861137.1:p.Ala804Thr
XM_017005650.1:c.2608G>A	XP_016861139.1:p.Ala870Thr
XM_017005651.1:c.2335G>A	XP_016861140.1:p.Ala779Thr
XM_017005652.1:c.2608G>A	XP_016861141.1:p.Ala870Thr
XM_017005653.1:c.1012G>A	XP_016861142.1:p.Ala338Thr
NM_001349253.2:c.2608G>A MANE Select	NP_001336182.1:p.Ala870Thr
NM_014139.3:c.2608G>A	NP_054858.2:p.Ala870Thr