Canonical Allele Identifier: CA1304976561
Gene: SCN9A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166303397A= , CM000664.2:g.166303397A= GRCh38
NC_000002.11:g.167159907A= , CM000664.1:g.167159907A= GRCh37
NC_000002.10:g.166868153A= NCBI36
NG_012798.1:g.77591T= , LRG_369:g.77591T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303354.11:c.689-95T= ENSP00000304748.7:n.689-95T=
ENST00000409435.6:c.689-95T= ENSP00000386330.2:n.689-95T=
ENST00000452182.2:c.689-95T= ENSP00000393141.2:n.689-95T=
ENST00000454569.6:c.689-95T= ENSP00000413212.2:n.689-95T=
ENST00000472119.2:n.1044-95T=
ENST00000642356.2:c.689-95T= MANE Select ENSP00000495601.1:n.689-95T=
ENST00000644316.1:c.689-95T= ENSP00000493939.1:n.689-95T=
ENST00000645815.1:n.60-95T=
ENST00000645907.1:c.689-95T= ENSP00000495983.1:n.689-95T=
ENST00000303354.10:c.689-95T= ENSP00000304748.7:n.689-95T=
ENST00000409435.5:c.689-95T= ENSP00000386330.1:n.689-95T=
ENST00000409672.5:c.689-95T= ENSP00000386306.1:n.689-95T=
ENST00000452182.1:c.284-95T= ENSP00000393141.1:n.284-95T=
ENST00000454569.5:c.284-95T= ENSP00000413212.1:n.284-95T=
ENST00000472119.1:n.222-95T=
NM_002977.3:c.689-95T= , LRG_369t1:c.689-95T= NP_002968.1:n.689-95T=
XM_005246757.1:c.689-95T= XP_005246814.1:n.689-95T=
XM_011511616.1:c.689-95T= XP_011509918.1:n.689-95T=
XM_011511617.1:c.689-95T= XP_011509919.1:n.689-95T=
XM_011511618.1:c.689-95T= XP_011509920.1:n.689-95T=
XM_011511619.1:c.689-95T= XP_011509921.1:n.689-95T=
NM_001365536.1:c.689-95T= MANE Select NP_001352465.1:n.689-95T=
XM_011511616.3:c.689-95T= XP_011509918.1:n.689-95T=
XM_011511617.2:c.689-95T= XP_011509919.1:n.689-95T=
XM_011511618.2:c.689-95T= XP_011509920.1:n.689-95T=
XM_011511619.2:c.689-95T= XP_011509921.1:n.689-95T=
XM_017004668.1:c.302-95T= XP_016860157.1:n.302-95T=
XM_017004669.1:c.-56-95T= XP_016860158.1:n.-56-95T=
XR_001738886.1:n.1003-95T=