Canonical Allele Identifier: CA10612520
Gene: SCN9A HGNC NCBI
SCN1A-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 331949
dbSNP Id: rs115464654

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166198295G>C , CM000664.2:g.166198295G>C GRCh38
NC_000002.11:g.167054805G>C , CM000664.1:g.167054805G>C GRCh37
NC_000002.10:g.166763051G>C NCBI36
NG_012798.1:g.182693C>G , LRG_369:g.182693C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000303354.11:c.*377C>G (SCN9A) ENSP00000304748.7:n.*377C>G
ENST00000642356.2:c.*377C>G (SCN9A) MANE Select ENSP00000495601.1:n.*377C>G
ENST00000645907.1:c.*377C>G (SCN9A) ENSP00000495983.1:n.*377C>G
ENST00000303354.10:c.*377C>G (SCN9A) ENSP00000304748.7:n.*377C>G
ENST00000409672.5:c.*377C>G (SCN9A) ENSP00000386306.1:n.*377C>G
NM_002977.3:c.*377C>G , LRG_369t1:c.*377C>G (SCN9A) NP_002968.1:n.*377C>G
NR_110260.1:n.432-1344G>C (SCN1A-AS1)
XM_005246757.1:c.*377C>G (SCN9A) XP_005246814.1:n.*377C>G
XM_011511616.1:c.*377C>G (SCN9A) XP_011509918.1:n.*377C>G
XM_011511617.1:c.*377C>G (SCN9A) XP_011509919.1:n.*377C>G
XM_011511618.1:c.*377C>G (SCN9A) XP_011509920.1:n.*377C>G
NM_001365536.1:c.*377C>G (SCN9A) MANE Select NP_001352465.1:n.*377C>G