Canonical Allele Identifier: CA2753033501

Gene: SCN9A SCN1A-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166288110_166288111insTT , CM000664.2:g.166288110_166288111insTT	GRCh38
NC_000002.11:g.167144620_167144621insTT , CM000664.1:g.167144620_167144621insTT	GRCh37
NC_000002.10:g.166852866_166852867insTT	NCBI36
NG_012798.1:g.92878_92879insAA , LRG_369:g.92878_92879insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303354.11:c.1314+327_1314+328insAA (SCN9A)	ENSP00000304748.7:n.1314+327_1314+328insAA
ENST00000409435.6:c.1314+327_1314+328insAA (SCN9A)	ENSP00000386330.2:n.1314+327_1314+328insAA
ENST00000454569.6:c.1314+327_1314+328insAA (SCN9A)	ENSP00000413212.2:n.1314+327_1314+328insAA
ENST00000642356.2:c.1314+327_1314+328insAA (SCN9A) MANE Select	ENSP00000495601.1:n.1314+327_1314+328insAA
ENST00000644316.1:c.1314+327_1314+328insAA (SCN9A)	ENSP00000493939.1:n.1314+327_1314+328insAA
ENST00000645907.1:c.1314+327_1314+328insAA (SCN9A)	ENSP00000495983.1:n.1314+327_1314+328insAA
ENST00000667201.2:c.349+327_349+328insAA (SCN9A)
ENST00000303354.10:c.1314+327_1314+328insAA (SCN9A)	ENSP00000304748.7:n.1314+327_1314+328insAA
ENST00000409435.5:c.1314+327_1314+328insAA (SCN9A)	ENSP00000386330.1:n.1314+327_1314+328insAA
ENST00000409672.5:c.1314+327_1314+328insAA (SCN9A)	ENSP00000386306.1:n.1314+327_1314+328insAA
ENST00000452182.1:c.909+327_909+328insAA (SCN9A)	ENSP00000393141.1:n.909+327_909+328insAA
ENST00000454569.5:c.909+327_909+328insAA (SCN9A)	ENSP00000413212.1:n.909+327_909+328insAA
NM_002977.3:c.1314+327_1314+328insAA , LRG_369t1:c.1314+327_1314+328insAA (SCN9A)	NP_002968.1:n.1314+327_1314+328insAA
NR_110260.1:n.1030-6455_1030-6454insTT (SCN1A-AS1)
XM_005246757.1:c.1314+327_1314+328insAA (SCN9A)	XP_005246814.1:n.1314+327_1314+328insAA
XM_011511616.1:c.1314+327_1314+328insAA (SCN9A)	XP_011509918.1:n.1314+327_1314+328insAA
XM_011511617.1:c.1314+327_1314+328insAA (SCN9A)	XP_011509919.1:n.1314+327_1314+328insAA
XM_011511618.1:c.1314+327_1314+328insAA (SCN9A)	XP_011509920.1:n.1314+327_1314+328insAA
XM_011511619.1:c.1314+327_1314+328insAA (SCN9A)	XP_011509921.1:n.1314+327_1314+328insAA
NM_001365536.1:c.1314+327_1314+328insAA (SCN9A) MANE Select	NP_001352465.1:n.1314+327_1314+328insAA
XM_011511616.3:c.1314+327_1314+328insAA (SCN9A)	XP_011509918.1:n.1314+327_1314+328insAA
XM_011511617.2:c.1314+327_1314+328insAA (SCN9A)	XP_011509919.1:n.1314+327_1314+328insAA
XM_011511618.2:c.1314+327_1314+328insAA (SCN9A)	XP_011509920.1:n.1314+327_1314+328insAA
XM_011511619.2:c.1314+327_1314+328insAA (SCN9A)	XP_011509921.1:n.1314+327_1314+328insAA
XM_017004668.1:c.927+327_927+328insAA (SCN9A)	XP_016860157.1:n.927+327_927+328insAA
XM_017004669.1:c.570+327_570+328insAA (SCN9A)	XP_016860158.1:n.570+327_570+328insAA
XR_001738886.1:n.1628+327_1628+328insAA (SCN9A)