Linked Data
dbSNP Id:
rs67284979
MyVariant Identifiers:
chr2:g.167089714_167089715insTATG (hg19)
chr2:g.166233204_166233205insTATG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.166233204_166233205insTATG , CM000664.2:g.166233204_166233205insTATG | GRCh38 |
| NC_000002.11:g.167089714_167089715insTATG , CM000664.1:g.167089714_167089715insTATG | GRCh37 |
| NC_000002.10:g.166797960_166797961insTATG | NCBI36 |
| NG_012798.1:g.147783_147784insCATA , LRG_369:g.147783_147784insCATA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303354.11:c.3924+135_3924+136insCATA (SCN9A) | ENSP00000304748.7:n.3924+135_3924+136insCATA | |
| ENST00000409435.6:c.3924+135_3924+136insCATA (SCN9A) | ENSP00000386330.2:n.3924+135_3924+136insCATA | |
| ENST00000642356.2:c.3924+135_3924+136insCATA (SCN9A) MANE Select | ENSP00000495601.1:n.3924+135_3924+136insCATA | |
| ENST00000644316.1:c.3769-4233_3769-4232insCATA (SCN9A) | ENSP00000493939.1:n.3769-4233_3769-4232insCATA | |
| ENST00000645907.1:c.3891+135_3891+136insCATA (SCN9A) | ENSP00000495983.1:n.3891+135_3891+136insCATA | |
| ENST00000303354.10:c.3924+135_3924+136insCATA (SCN9A) | ENSP00000304748.7:n.3924+135_3924+136insCATA | |
| ENST00000409435.5:c.3924+135_3924+136insCATA (SCN9A) | ENSP00000386330.1:n.3924+135_3924+136insCATA | |
| ENST00000409672.5:c.3891+135_3891+136insCATA (SCN9A) | ENSP00000386306.1:n.3891+135_3891+136insCATA | |
| NM_002977.3:c.3891+135_3891+136insCATA , LRG_369t1:c.3891+135_3891+136insCATA (SCN9A) | NP_002968.1:n.3891+135_3891+136insCATA | |
| NR_110260.1:n.612-14991_612-14990insTATG (SCN1A-AS1) | ||
| XM_005246757.1:c.3924+135_3924+136insCATA (SCN9A) | XP_005246814.1:n.3924+135_3924+136insCATA | |
| XM_011511616.1:c.3924+135_3924+136insCATA (SCN9A) | XP_011509918.1:n.3924+135_3924+136insCATA | |
| XM_011511617.1:c.3924+135_3924+136insCATA (SCN9A) | XP_011509919.1:n.3924+135_3924+136insCATA | |
| XM_011511618.1:c.3891+135_3891+136insCATA (SCN9A) | XP_011509920.1:n.3891+135_3891+136insCATA | |
| XM_011511619.1:c.3924+135_3924+136insCATA (SCN9A) | XP_011509921.1:n.3924+135_3924+136insCATA | |
| NM_001365536.1:c.3924+135_3924+136insCATA (SCN9A) MANE Select | NP_001352465.1:n.3924+135_3924+136insCATA | |
| XM_011511616.3:c.3924+135_3924+136insCATA (SCN9A) | XP_011509918.1:n.3924+135_3924+136insCATA | |
| XM_011511617.2:c.3924+135_3924+136insCATA (SCN9A) | XP_011509919.1:n.3924+135_3924+136insCATA | |
| XM_011511618.2:c.3891+135_3891+136insCATA (SCN9A) | XP_011509920.1:n.3891+135_3891+136insCATA | |
| XM_011511619.2:c.3924+135_3924+136insCATA (SCN9A) | XP_011509921.1:n.3924+135_3924+136insCATA | |
| XM_017004668.1:c.3537+135_3537+136insCATA (SCN9A) | XP_016860157.1:n.3537+135_3537+136insCATA | |
| XM_017004669.1:c.3180+135_3180+136insCATA (SCN9A) | XP_016860158.1:n.3180+135_3180+136insCATA |