Canonical Allele Identifier: CA537525995

Gene: SCN9A SCN1A-AS1

Linked Data

• dbSNP Id: rs1279631698
• gnomAD v2: 2-167144622-T-TAC
• gnomAD v3: 2-166288112-T-TAC
• gnomAD v4: 2-166288112-T-TAC
• MyVariant Identifiers: chr2:g.167144622_167144623insAC (hg19) ; chr2:g.166288112_166288113insAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166288113_166288114insCA , CM000664.2:g.166288113_166288114insCA	GRCh38
NC_000002.11:g.167144623_167144624insCA , CM000664.1:g.167144623_167144624insCA	GRCh37
NC_000002.10:g.166852869_166852870insCA	NCBI36
NG_012798.1:g.92875_92876insGT , LRG_369:g.92875_92876insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303354.11:c.1314+324_1314+325insGT (SCN9A)	ENSP00000304748.7:n.1314+324_1314+325insGT
ENST00000409435.6:c.1314+324_1314+325insGT (SCN9A)	ENSP00000386330.2:n.1314+324_1314+325insGT
ENST00000454569.6:c.1314+324_1314+325insGT (SCN9A)	ENSP00000413212.2:n.1314+324_1314+325insGT
ENST00000642356.2:c.1314+324_1314+325insGT (SCN9A) MANE Select	ENSP00000495601.1:n.1314+324_1314+325insGT
ENST00000644316.1:c.1314+324_1314+325insGT (SCN9A)	ENSP00000493939.1:n.1314+324_1314+325insGT
ENST00000645907.1:c.1314+324_1314+325insGT (SCN9A)	ENSP00000495983.1:n.1314+324_1314+325insGT
ENST00000667201.2:c.349+324_349+325insGT (SCN9A)
ENST00000303354.10:c.1314+324_1314+325insGT (SCN9A)	ENSP00000304748.7:n.1314+324_1314+325insGT
ENST00000409435.5:c.1314+324_1314+325insGT (SCN9A)	ENSP00000386330.1:n.1314+324_1314+325insGT
ENST00000409672.5:c.1314+324_1314+325insGT (SCN9A)	ENSP00000386306.1:n.1314+324_1314+325insGT
ENST00000452182.1:c.909+324_909+325insGT (SCN9A)	ENSP00000393141.1:n.909+324_909+325insGT
ENST00000454569.5:c.909+324_909+325insGT (SCN9A)	ENSP00000413212.1:n.909+324_909+325insGT
NM_002977.3:c.1314+324_1314+325insGT , LRG_369t1:c.1314+324_1314+325insGT (SCN9A)	NP_002968.1:n.1314+324_1314+325insGT
NR_110260.1:n.1030-6452_1030-6451insCA (SCN1A-AS1)
XM_005246757.1:c.1314+324_1314+325insGT (SCN9A)	XP_005246814.1:n.1314+324_1314+325insGT
XM_011511616.1:c.1314+324_1314+325insGT (SCN9A)	XP_011509918.1:n.1314+324_1314+325insGT
XM_011511617.1:c.1314+324_1314+325insGT (SCN9A)	XP_011509919.1:n.1314+324_1314+325insGT
XM_011511618.1:c.1314+324_1314+325insGT (SCN9A)	XP_011509920.1:n.1314+324_1314+325insGT
XM_011511619.1:c.1314+324_1314+325insGT (SCN9A)	XP_011509921.1:n.1314+324_1314+325insGT
NM_001365536.1:c.1314+324_1314+325insGT (SCN9A) MANE Select	NP_001352465.1:n.1314+324_1314+325insGT
XM_011511616.3:c.1314+324_1314+325insGT (SCN9A)	XP_011509918.1:n.1314+324_1314+325insGT
XM_011511617.2:c.1314+324_1314+325insGT (SCN9A)	XP_011509919.1:n.1314+324_1314+325insGT
XM_011511618.2:c.1314+324_1314+325insGT (SCN9A)	XP_011509920.1:n.1314+324_1314+325insGT
XM_011511619.2:c.1314+324_1314+325insGT (SCN9A)	XP_011509921.1:n.1314+324_1314+325insGT
XM_017004668.1:c.927+324_927+325insGT (SCN9A)	XP_016860157.1:n.927+324_927+325insGT
XM_017004669.1:c.570+324_570+325insGT (SCN9A)	XP_016860158.1:n.570+324_570+325insGT
XR_001738886.1:n.1628+324_1628+325insGT (SCN9A)