Canonical Allele Identifier: CA10611647
Gene: SCN9A HGNC NCBI
SCN1A-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 331959
dbSNP Id: rs201137748

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166198548T>C , CM000664.2:g.166198548T>C GRCh38
NC_000002.11:g.167055058T>C , CM000664.1:g.167055058T>C GRCh37
NC_000002.10:g.166763304T>C NCBI36
NG_012798.1:g.182440A>G , LRG_369:g.182440A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000303354.11:c.*124A>G (SCN9A) ENSP00000304748.7:n.*124A>G
ENST00000642356.2:c.*124A>G (SCN9A) MANE Select ENSP00000495601.1:n.*124A>G
ENST00000644316.1:c.5935A>G (SCN9A) ENSP00000493939.1:n.5935A>G
ENST00000645907.1:c.*124A>G (SCN9A) ENSP00000495983.1:n.*124A>G
ENST00000646694.1:n.2468A>G (SCN9A)
ENST00000303354.10:c.*124A>G (SCN9A) ENSP00000304748.7:n.*124A>G
ENST00000409672.5:c.*124A>G (SCN9A) ENSP00000386306.1:n.*124A>G
NM_002977.3:c.*124A>G , LRG_369t1:c.*124A>G (SCN9A) NP_002968.1:n.*124A>G
NR_110260.1:n.432-1091T>C (SCN1A-AS1)
XM_005246757.1:c.*124A>G (SCN9A) XP_005246814.1:n.*124A>G
XM_011511616.1:c.*124A>G (SCN9A) XP_011509918.1:n.*124A>G
XM_011511617.1:c.*124A>G (SCN9A) XP_011509919.1:n.*124A>G
XM_011511618.1:c.*124A>G (SCN9A) XP_011509920.1:n.*124A>G
NM_001365536.1:c.*124A>G (SCN9A) MANE Select NP_001352465.1:n.*124A>G