Canonical Allele Identifier: CA352171305

Gene: SCN11A

Linked Data

• MyVariant Identifiers: chr3:g.38913710C>G (hg19) ; chr3:g.38872219C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38872219C>G , CM000665.2:g.38872219C>G	GRCh38
NC_000003.11:g.38913710C>G , CM000665.1:g.38913710C>G	GRCh37
NC_000003.10:g.38888714C>G	NCBI36
NG_033859.1:g.83343G>C
NG_033859.2:g.184768G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302328.9:c.3469G>C MANE Select	ENSP00000307599.3:p.Ala1157Pro
ENST00000668754.1:c.3469G>C	ENSP00000499569.1:p.Ala1157Pro
ENST00000675223.1:c.3469G>C	ENSP00000502481.1:p.Ala1157Pro
ENST00000675672.1:c.3523G>C	ENSP00000502446.1:n.3523G>C
ENST00000675892.1:c.3289G>C	ENSP00000502318.1:p.Ala1097Pro
ENST00000676045.1:c.3513G>C	ENSP00000501685.1:n.3513G>C
ENST00000676176.1:c.3088G>C	ENSP00000501891.1:p.Ala1030Pro
ENST00000302328.7:c.3469G>C	ENSP00000307599.3:p.Ala1157Pro
ENST00000444237.2:c.3469G>C	ENSP00000408028.2:p.Ala1157Pro
ENST00000456224.7:c.3355G>C	ENSP00000416757.3:p.Ala1119Pro
NM_001287223.1:c.3469G>C	NP_001274152.1:p.Ala1157Pro
NM_014139.2:c.3469G>C	NP_054858.2:p.Ala1157Pro
XM_011533320.1:c.3469G>C	XP_011531622.1:p.Ala1157Pro
XM_011533321.1:c.2806G>C	XP_011531623.1:p.Ala936Pro
XM_011533322.1:c.2017G>C	XP_011531624.1:p.Ala673Pro
NM_001349253.1:c.3469G>C	NP_001336182.1:p.Ala1157Pro
XM_011533321.2:c.2806G>C	XP_011531623.1:p.Ala936Pro
XM_017005647.1:c.3844G>C	XP_016861136.1:p.Ala1282Pro
XM_017005648.1:c.3271G>C	XP_016861137.1:p.Ala1091Pro
XM_017005650.1:c.3469G>C	XP_016861139.1:p.Ala1157Pro
XM_017005651.1:c.3196G>C	XP_016861140.1:p.Ala1066Pro
XM_017005652.1:c.3469G>C	XP_016861141.1:p.Ala1157Pro
XM_017005653.1:c.1873G>C	XP_016861142.1:p.Ala625Pro
NM_001349253.2:c.3469G>C MANE Select	NP_001336182.1:p.Ala1157Pro
NM_014139.3:c.3469G>C	NP_054858.2:p.Ala1157Pro