Canonical Allele Identifier: CA352171307

Gene: SCN11A

Linked Data

• MyVariant Identifiers: chr3:g.38913712C>G (hg19) ; chr3:g.38872221C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38872221C>G , CM000665.2:g.38872221C>G	GRCh38
NC_000003.11:g.38913712C>G , CM000665.1:g.38913712C>G	GRCh37
NC_000003.10:g.38888716C>G	NCBI36
NG_033859.1:g.83341G>C
NG_033859.2:g.184766G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302328.9:c.3467G>C MANE Select	ENSP00000307599.3:p.Arg1156Pro
ENST00000668754.1:c.3467G>C	ENSP00000499569.1:p.Arg1156Pro
ENST00000675223.1:c.3467G>C	ENSP00000502481.1:p.Arg1156Pro
ENST00000675672.1:c.3521G>C	ENSP00000502446.1:n.3521G>C
ENST00000675892.1:c.3287G>C	ENSP00000502318.1:p.Arg1096Pro
ENST00000676045.1:c.3511G>C	ENSP00000501685.1:n.3511G>C
ENST00000676176.1:c.3086G>C	ENSP00000501891.1:p.Arg1029Pro
ENST00000302328.7:c.3467G>C	ENSP00000307599.3:p.Arg1156Pro
ENST00000444237.2:c.3467G>C	ENSP00000408028.2:p.Arg1156Pro
ENST00000456224.7:c.3353G>C	ENSP00000416757.3:p.Arg1118Pro
NM_001287223.1:c.3467G>C	NP_001274152.1:p.Arg1156Pro
NM_014139.2:c.3467G>C	NP_054858.2:p.Arg1156Pro
XM_011533320.1:c.3467G>C	XP_011531622.1:p.Arg1156Pro
XM_011533321.1:c.2804G>C	XP_011531623.1:p.Arg935Pro
XM_011533322.1:c.2015G>C	XP_011531624.1:p.Arg672Pro
NM_001349253.1:c.3467G>C	NP_001336182.1:p.Arg1156Pro
XM_011533321.2:c.2804G>C	XP_011531623.1:p.Arg935Pro
XM_017005647.1:c.3842G>C	XP_016861136.1:p.Arg1281Pro
XM_017005648.1:c.3269G>C	XP_016861137.1:p.Arg1090Pro
XM_017005650.1:c.3467G>C	XP_016861139.1:p.Arg1156Pro
XM_017005651.1:c.3194G>C	XP_016861140.1:p.Arg1065Pro
XM_017005652.1:c.3467G>C	XP_016861141.1:p.Arg1156Pro
XM_017005653.1:c.1871G>C	XP_016861142.1:p.Arg624Pro
NM_001349253.2:c.3467G>C MANE Select	NP_001336182.1:p.Arg1156Pro
NM_014139.3:c.3467G>C	NP_054858.2:p.Arg1156Pro