Canonical Allele Identifier: CA349092643
Gene: SCN9A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166303169T>A , CM000664.2:g.166303169T>A GRCh38
NC_000002.11:g.167159679T>A , CM000664.1:g.167159679T>A GRCh37
NC_000002.10:g.166867925T>A NCBI36
NG_012798.1:g.77819A>T , LRG_369:g.77819A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000303354.11:c.822A>T ENSP00000304748.7:p.Lys274Asn
ENST00000409435.6:c.822A>T ENSP00000386330.2:p.Lys274Asn
ENST00000452182.2:c.822A>T ENSP00000393141.2:p.Lys274Asn
ENST00000454569.6:c.822A>T ENSP00000413212.2:p.Lys274Asn
ENST00000472119.2:n.1177A>T
ENST00000642356.2:c.822A>T MANE Select ENSP00000495601.1:p.Lys274Asn
ENST00000644316.1:c.822A>T ENSP00000493939.1:p.Lys274Asn
ENST00000645815.1:n.193A>T
ENST00000645907.1:c.822A>T ENSP00000495983.1:p.Lys274Asn
ENST00000303354.10:c.822A>T ENSP00000304748.7:p.Lys274Asn
ENST00000409435.5:c.822A>T ENSP00000386330.1:p.Lys274Asn
ENST00000409672.5:c.822A>T ENSP00000386306.1:p.Lys274Asn
ENST00000452182.1:c.417A>T ENSP00000393141.1:p.Lys139Asn
ENST00000454569.5:c.417A>T ENSP00000413212.1:p.Lys139Asn
ENST00000472119.1:n.355A>T
NM_002977.3:c.822A>T , LRG_369t1:c.822A>T NP_002968.1:p.Lys274Asn
XM_005246757.1:c.822A>T XP_005246814.1:p.Lys274Asn
XM_011511616.1:c.822A>T XP_011509918.1:p.Lys274Asn
XM_011511617.1:c.822A>T XP_011509919.1:p.Lys274Asn
XM_011511618.1:c.822A>T XP_011509920.1:p.Lys274Asn
XM_011511619.1:c.822A>T XP_011509921.1:p.Lys274Asn
NM_001365536.1:c.822A>T MANE Select NP_001352465.1:p.Lys274Asn
XM_011511616.3:c.822A>T XP_011509918.1:p.Lys274Asn
XM_011511617.2:c.822A>T XP_011509919.1:p.Lys274Asn
XM_011511618.2:c.822A>T XP_011509920.1:p.Lys274Asn
XM_011511619.2:c.822A>T XP_011509921.1:p.Lys274Asn
XM_017004668.1:c.435A>T XP_016860157.1:p.Lys145Asn
XM_017004669.1:c.78A>T XP_016860158.1:p.Lys26Asn
XR_001738886.1:n.1136A>T