Canonical Allele Identifier: CA1944192
Gene: SCN9A HGNC NCBI
SCN1A-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs775257309

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166277000C>A , CM000664.2:g.166277000C>A GRCh38
NC_000002.11:g.167133510C>A , CM000664.1:g.167133510C>A GRCh37
NC_000002.10:g.166841756C>A NCBI36
NG_012798.1:g.103988G>T , LRG_369:g.103988G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000303354.11:c.2857G>T (SCN9A) ENSP00000304748.7:p.Val953Phe
ENST00000409435.6:c.2857G>T (SCN9A) ENSP00000386330.2:p.Val953Phe
ENST00000642356.2:c.2857G>T (SCN9A) MANE Select ENSP00000495601.1:p.Val953Phe
ENST00000644316.1:c.2824G>T (SCN9A) ENSP00000493939.1:p.Val942Phe
ENST00000645283.1:c.514G>T (SCN9A) ENSP00000496086.1:p.Val172Phe
ENST00000645907.1:c.2824G>T (SCN9A) ENSP00000495983.1:p.Val942Phe
ENST00000667201.2:c.1859G>T (SCN9A)
ENST00000303354.10:c.2857G>T (SCN9A) ENSP00000304748.7:p.Val953Phe
ENST00000409435.5:c.2857G>T (SCN9A) ENSP00000386330.1:p.Val953Phe
ENST00000409672.5:c.2824G>T (SCN9A) ENSP00000386306.1:p.Val942Phe
NM_002977.3:c.2824G>T , LRG_369t1:c.2824G>T (SCN9A) NP_002968.1:p.Val942Phe
NR_110260.1:n.870-88C>A (SCN1A-AS1)
XM_005246757.1:c.2857G>T (SCN9A) XP_005246814.1:p.Val953Phe
XM_011511616.1:c.2857G>T (SCN9A) XP_011509918.1:p.Val953Phe
XM_011511617.1:c.2857G>T (SCN9A) XP_011509919.1:p.Val953Phe
XM_011511618.1:c.2824G>T (SCN9A) XP_011509920.1:p.Val942Phe
XM_011511619.1:c.2857G>T (SCN9A) XP_011509921.1:p.Val953Phe
NM_001365536.1:c.2857G>T (SCN9A) MANE Select NP_001352465.1:p.Val953Phe
XM_011511616.3:c.2857G>T (SCN9A) XP_011509918.1:p.Val953Phe
XM_011511617.2:c.2857G>T (SCN9A) XP_011509919.1:p.Val953Phe
XM_011511618.2:c.2824G>T (SCN9A) XP_011509920.1:p.Val942Phe
XM_011511619.2:c.2857G>T (SCN9A) XP_011509921.1:p.Val953Phe
XM_017004668.1:c.2470G>T (SCN9A) XP_016860157.1:p.Val824Phe
XM_017004669.1:c.2113G>T (SCN9A) XP_016860158.1:p.Val705Phe
XR_001738886.1:n.3171G>T (SCN9A)