Canonical Allele Identifier: CA2740339108
Gene: SCN9A HGNC NCBI
SCN1A-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166228676_166228677insT , CM000664.2:g.166228676_166228677insT GRCh38
NC_000002.11:g.167085186_167085187insT , CM000664.1:g.167085186_167085187insT GRCh37
NC_000002.10:g.166793432_166793433insT NCBI36
NG_012798.1:g.152311_152312insA , LRG_369:g.152311_152312insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000303354.11:c.4206+14_4206+15insA (SCN9A) ENSP00000304748.7:n.4206+14_4206+15insA
ENST00000409435.6:c.4206+14_4206+15insA (SCN9A) ENSP00000386330.2:n.4206+14_4206+15insA
ENST00000642356.2:c.4206+14_4206+15insA (SCN9A) MANE Select ENSP00000495601.1:n.4206+14_4206+15insA
ENST00000644316.1:c.4050+14_4050+15insA (SCN9A) ENSP00000493939.1:n.4050+14_4050+15insA
ENST00000645907.1:c.4173+14_4173+15insA (SCN9A) ENSP00000495983.1:n.4173+14_4173+15insA
ENST00000303354.10:c.4206+14_4206+15insA (SCN9A) ENSP00000304748.7:n.4206+14_4206+15insA
ENST00000409435.5:c.4206+14_4206+15insA (SCN9A) ENSP00000386330.1:n.4206+14_4206+15insA
ENST00000409672.5:c.4173+14_4173+15insA (SCN9A) ENSP00000386306.1:n.4173+14_4173+15insA
NM_002977.3:c.4173+14_4173+15insA , LRG_369t1:c.4173+14_4173+15insA (SCN9A) NP_002968.1:n.4173+14_4173+15insA
NR_110260.1:n.612-19519_612-19518insT (SCN1A-AS1)
XM_005246757.1:c.4206+14_4206+15insA (SCN9A) XP_005246814.1:n.4206+14_4206+15insA
XM_011511616.1:c.4206+14_4206+15insA (SCN9A) XP_011509918.1:n.4206+14_4206+15insA
XM_011511617.1:c.4206+14_4206+15insA (SCN9A) XP_011509919.1:n.4206+14_4206+15insA
XM_011511618.1:c.4173+14_4173+15insA (SCN9A) XP_011509920.1:n.4173+14_4173+15insA
XM_011511619.1:c.4206+14_4206+15insA (SCN9A) XP_011509921.1:n.4206+14_4206+15insA
NM_001365536.1:c.4206+14_4206+15insA (SCN9A) MANE Select NP_001352465.1:n.4206+14_4206+15insA
XM_011511616.3:c.4206+14_4206+15insA (SCN9A) XP_011509918.1:n.4206+14_4206+15insA
XM_011511617.2:c.4206+14_4206+15insA (SCN9A) XP_011509919.1:n.4206+14_4206+15insA
XM_011511618.2:c.4173+14_4173+15insA (SCN9A) XP_011509920.1:n.4173+14_4173+15insA
XM_011511619.2:c.4206+14_4206+15insA (SCN9A) XP_011509921.1:n.4206+14_4206+15insA
XM_017004668.1:c.3819+14_3819+15insA (SCN9A) XP_016860157.1:n.3819+14_3819+15insA
XM_017004669.1:c.3462+14_3462+15insA (SCN9A) XP_016860158.1:n.3462+14_3462+15insA