Canonical Allele Identifier: CA1304984768

Gene: SCN9A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166320869C= , CM000664.2:g.166320869C=	GRCh38
NC_000002.11:g.167177379C= , CM000664.1:g.167177379C=	GRCh37
NC_000002.10:g.166885625C=	NCBI36
NG_012798.1:g.60119G= , LRG_369:g.60119G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000303354.11:c.-50-9063G=	ENSP00000304748.7:n.-50-9063G=
ENST00000452182.2:c.-51+570G=	ENSP00000393141.2:n.-51+570G=
ENST00000454569.6:c.-50-9063G=	ENSP00000413212.2:n.-50-9063G=
ENST00000472119.2:n.306-9063G=
ENST00000642356.2:c.-50-9063G= MANE Select	ENSP00000495601.1:n.-50-9063G=
ENST00000645907.1:c.-50-9063G=	ENSP00000495983.1:n.-50-9063G=
ENST00000303354.10:c.-50-9063G=	ENSP00000304748.7:n.-50-9063G=
ENST00000409672.5:c.-50-9063G=	ENSP00000386306.1:n.-50-9063G=
NM_002977.3:c.-50-9063G= , LRG_369t1:c.-50-9063G=	NP_002968.1:n.-50-9063G=
XM_005246757.1:c.-50-9063G=	XP_005246814.1:n.-50-9063G=
XM_011511616.1:c.-50-9063G=	XP_011509918.1:n.-50-9063G=
XM_011511617.1:c.-50-9063G=	XP_011509919.1:n.-50-9063G=
XM_011511618.1:c.-50-9063G=	XP_011509920.1:n.-50-9063G=
XM_011511619.1:c.-50-9063G=	XP_011509921.1:n.-50-9063G=
NM_001365536.1:c.-50-9063G= MANE Select	NP_001352465.1:n.-50-9063G=
XM_011511616.3:c.-50-9063G=	XP_011509918.1:n.-50-9063G=
XM_011511617.2:c.-50-9063G=	XP_011509919.1:n.-50-9063G=
XM_011511618.2:c.-50-9063G=	XP_011509920.1:n.-50-9063G=
XM_011511619.2:c.-50-9063G=	XP_011509921.1:n.-50-9063G=
XR_001738886.1:n.265-9063G=