Canonical Allele Identifier: CA537525991

Gene: SCN9A SCN1A-AS1

Linked Data

• gnomAD v2: 2-167144613-A-ATC
• MyVariant Identifiers: chr2:g.167144613_167144614insTC (hg19) ; chr2:g.166288103_166288104insTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166288104_166288105insCT , CM000664.2:g.166288104_166288105insCT	GRCh38
NC_000002.11:g.167144614_167144615insCT , CM000664.1:g.167144614_167144615insCT	GRCh37
NC_000002.10:g.166852860_166852861insCT	NCBI36
NG_012798.1:g.92884_92885insGA , LRG_369:g.92884_92885insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303354.11:c.1314+333_1314+334insGA (SCN9A)	ENSP00000304748.7:n.1314+333_1314+334insGA
ENST00000409435.6:c.1314+333_1314+334insGA (SCN9A)	ENSP00000386330.2:n.1314+333_1314+334insGA
ENST00000454569.6:c.1314+333_1314+334insGA (SCN9A)	ENSP00000413212.2:n.1314+333_1314+334insGA
ENST00000642356.2:c.1314+333_1314+334insGA (SCN9A) MANE Select	ENSP00000495601.1:n.1314+333_1314+334insGA
ENST00000644316.1:c.1314+333_1314+334insGA (SCN9A)	ENSP00000493939.1:n.1314+333_1314+334insGA
ENST00000645907.1:c.1314+333_1314+334insGA (SCN9A)	ENSP00000495983.1:n.1314+333_1314+334insGA
ENST00000667201.2:c.349+333_349+334insGA (SCN9A)
ENST00000303354.10:c.1314+333_1314+334insGA (SCN9A)	ENSP00000304748.7:n.1314+333_1314+334insGA
ENST00000409435.5:c.1314+333_1314+334insGA (SCN9A)	ENSP00000386330.1:n.1314+333_1314+334insGA
ENST00000409672.5:c.1314+333_1314+334insGA (SCN9A)	ENSP00000386306.1:n.1314+333_1314+334insGA
ENST00000452182.1:c.909+333_909+334insGA (SCN9A)	ENSP00000393141.1:n.909+333_909+334insGA
ENST00000454569.5:c.909+333_909+334insGA (SCN9A)	ENSP00000413212.1:n.909+333_909+334insGA
NM_002977.3:c.1314+333_1314+334insGA , LRG_369t1:c.1314+333_1314+334insGA (SCN9A)	NP_002968.1:n.1314+333_1314+334insGA
NR_110260.1:n.1030-6461_1030-6460insCT (SCN1A-AS1)
XM_005246757.1:c.1314+333_1314+334insGA (SCN9A)	XP_005246814.1:n.1314+333_1314+334insGA
XM_011511616.1:c.1314+333_1314+334insGA (SCN9A)	XP_011509918.1:n.1314+333_1314+334insGA
XM_011511617.1:c.1314+333_1314+334insGA (SCN9A)	XP_011509919.1:n.1314+333_1314+334insGA
XM_011511618.1:c.1314+333_1314+334insGA (SCN9A)	XP_011509920.1:n.1314+333_1314+334insGA
XM_011511619.1:c.1314+333_1314+334insGA (SCN9A)	XP_011509921.1:n.1314+333_1314+334insGA
NM_001365536.1:c.1314+333_1314+334insGA (SCN9A) MANE Select	NP_001352465.1:n.1314+333_1314+334insGA
XM_011511616.3:c.1314+333_1314+334insGA (SCN9A)	XP_011509918.1:n.1314+333_1314+334insGA
XM_011511617.2:c.1314+333_1314+334insGA (SCN9A)	XP_011509919.1:n.1314+333_1314+334insGA
XM_011511618.2:c.1314+333_1314+334insGA (SCN9A)	XP_011509920.1:n.1314+333_1314+334insGA
XM_011511619.2:c.1314+333_1314+334insGA (SCN9A)	XP_011509921.1:n.1314+333_1314+334insGA
XM_017004668.1:c.927+333_927+334insGA (SCN9A)	XP_016860157.1:n.927+333_927+334insGA
XM_017004669.1:c.570+333_570+334insGA (SCN9A)	XP_016860158.1:n.570+333_570+334insGA
XR_001738886.1:n.1628+333_1628+334insGA (SCN9A)