Canonical Allele Identifier: CA1944569
Gene: SCN9A HGNC NCBI
SCN1A-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 471079
dbSNP Id: rs768527780

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166288547C>T , CM000664.2:g.166288547C>T GRCh38
NC_000002.11:g.167145057C>T , CM000664.1:g.167145057C>T GRCh37
NC_000002.10:g.166853303C>T NCBI36
NG_012798.1:g.92441G>A , LRG_369:g.92441G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000303354.11:c.1204G>A (SCN9A) ENSP00000304748.7:p.Ala402Thr
ENST00000409435.6:c.1204G>A (SCN9A) ENSP00000386330.2:p.Ala402Thr
ENST00000454569.6:c.1204G>A (SCN9A) ENSP00000413212.2:p.Ala402Thr
ENST00000642356.2:c.1204G>A (SCN9A) MANE Select ENSP00000495601.1:p.Ala402Thr
ENST00000644316.1:c.1204G>A (SCN9A) ENSP00000493939.1:p.Ala402Thr
ENST00000645907.1:c.1204G>A (SCN9A) ENSP00000495983.1:p.Ala402Thr
ENST00000667201.2:c.239G>A (SCN9A)
ENST00000303354.10:c.1204G>A (SCN9A) ENSP00000304748.7:p.Ala402Thr
ENST00000409435.5:c.1204G>A (SCN9A) ENSP00000386330.1:p.Ala402Thr
ENST00000409672.5:c.1204G>A (SCN9A) ENSP00000386306.1:p.Ala402Thr
ENST00000452182.1:c.799G>A (SCN9A) ENSP00000393141.1:p.Ala267Thr
ENST00000454569.5:c.799G>A (SCN9A) ENSP00000413212.1:p.Ala267Thr
NM_002977.3:c.1204G>A , LRG_369t1:c.1204G>A (SCN9A) NP_002968.1:p.Ala402Thr
NR_110260.1:n.1030-6018C>T (SCN1A-AS1)
XM_005246757.1:c.1204G>A (SCN9A) XP_005246814.1:p.Ala402Thr
XM_011511616.1:c.1204G>A (SCN9A) XP_011509918.1:p.Ala402Thr
XM_011511617.1:c.1204G>A (SCN9A) XP_011509919.1:p.Ala402Thr
XM_011511618.1:c.1204G>A (SCN9A) XP_011509920.1:p.Ala402Thr
XM_011511619.1:c.1204G>A (SCN9A) XP_011509921.1:p.Ala402Thr
NM_001365536.1:c.1204G>A (SCN9A) MANE Select NP_001352465.1:p.Ala402Thr
XM_011511616.3:c.1204G>A (SCN9A) XP_011509918.1:p.Ala402Thr
XM_011511617.2:c.1204G>A (SCN9A) XP_011509919.1:p.Ala402Thr
XM_011511618.2:c.1204G>A (SCN9A) XP_011509920.1:p.Ala402Thr
XM_011511619.2:c.1204G>A (SCN9A) XP_011509921.1:p.Ala402Thr
XM_017004668.1:c.817G>A (SCN9A) XP_016860157.1:p.Ala273Thr
XM_017004669.1:c.460G>A (SCN9A) XP_016860158.1:p.Ala154Thr
XR_001738886.1:n.1518G>A (SCN9A)