Canonical Allele Identifier: CA1304962916

Gene: SCN9A SCN1A-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166272913_166272923delinsAGACAGGAAAT , CM000664.2:g.166272913_166272923delinsAGACAGGAAAT	GRCh38
NC_000002.11:g.167129423_167129433delinsAGACAGGAAAT , CM000664.1:g.167129423_167129433delinsAGACAGGAAAT	GRCh37
NC_000002.10:g.166837669_166837679delinsAGACAGGAAAT	NCBI36
NG_012798.1:g.108065_108075delinsATTTCCTGTCT , LRG_369:g.108065_108075delinsATTTCCTGTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303354.11:c.2875-48_2875-38delinsATTTCCTGTCT (SCN9A)	ENSP00000304748.7:n.2875-48_2875-38delinsATTTCCTGTCT
ENST00000409435.6:c.2875-48_2875-38delinsATTTCCTGTCT (SCN9A)	ENSP00000386330.2:n.2875-48_2875-38delinsATTTCCTGTCT
ENST00000642356.2:c.2875-48_2875-38delinsATTTCCTGTCT (SCN9A) MANE Select	ENSP00000495601.1:n.2875-48_2875-38delinsATTTCCTGTCT
ENST00000644316.1:c.2842-48_2842-38delinsATTTCCTGTCT (SCN9A)	ENSP00000493939.1:n.2842-48_2842-38delinsATTTCCTGTCT
ENST00000645907.1:c.2842-48_2842-38delinsATTTCCTGTCT (SCN9A)	ENSP00000495983.1:n.2842-48_2842-38delinsATTTCCTGTCT
ENST00000667201.2:c.1877-425_1877-415delinsATTTCCTGTCT (SCN9A)
ENST00000303354.10:c.2875-48_2875-38delinsATTTCCTGTCT (SCN9A)	ENSP00000304748.7:n.2875-48_2875-38delinsATTTCCTGTCT
ENST00000409435.5:c.2875-48_2875-38delinsATTTCCTGTCT (SCN9A)	ENSP00000386330.1:n.2875-48_2875-38delinsATTTCCTGTCT
ENST00000409672.5:c.2842-48_2842-38delinsATTTCCTGTCT (SCN9A)	ENSP00000386306.1:n.2842-48_2842-38delinsATTTCCTGTCT
NM_002977.3:c.2842-48_2842-38delinsATTTCCTGTCT , LRG_369t1:c.2842-48_2842-38delinsATTTCCTGTCT (SCN9A)	NP_002968.1:n.2842-48_2842-38delinsATTTCCTGTCT
NR_110260.1:n.870-4175_870-4165delinsAGACAGGAAAT (SCN1A-AS1)
XM_005246757.1:c.2875-48_2875-38delinsATTTCCTGTCT (SCN9A)	XP_005246814.1:n.2875-48_2875-38delinsATTTCCTGTCT
XM_011511616.1:c.2875-48_2875-38delinsATTTCCTGTCT (SCN9A)	XP_011509918.1:n.2875-48_2875-38delinsATTTCCTGTCT
XM_011511617.1:c.2875-48_2875-38delinsATTTCCTGTCT (SCN9A)	XP_011509919.1:n.2875-48_2875-38delinsATTTCCTGTCT
XM_011511618.1:c.2842-48_2842-38delinsATTTCCTGTCT (SCN9A)	XP_011509920.1:n.2842-48_2842-38delinsATTTCCTGTCT
XM_011511619.1:c.2875-48_2875-38delinsATTTCCTGTCT (SCN9A)	XP_011509921.1:n.2875-48_2875-38delinsATTTCCTGTCT
NM_001365536.1:c.2875-48_2875-38delinsATTTCCTGTCT (SCN9A) MANE Select	NP_001352465.1:n.2875-48_2875-38delinsATTTCCTGTCT
XM_011511616.3:c.2875-48_2875-38delinsATTTCCTGTCT (SCN9A)	XP_011509918.1:n.2875-48_2875-38delinsATTTCCTGTCT
XM_011511617.2:c.2875-48_2875-38delinsATTTCCTGTCT (SCN9A)	XP_011509919.1:n.2875-48_2875-38delinsATTTCCTGTCT
XM_011511618.2:c.2842-48_2842-38delinsATTTCCTGTCT (SCN9A)	XP_011509920.1:n.2842-48_2842-38delinsATTTCCTGTCT
XM_011511619.2:c.2875-48_2875-38delinsATTTCCTGTCT (SCN9A)	XP_011509921.1:n.2875-48_2875-38delinsATTTCCTGTCT
XM_017004668.1:c.2488-48_2488-38delinsATTTCCTGTCT (SCN9A)	XP_016860157.1:n.2488-48_2488-38delinsATTTCCTGTCT
XM_017004669.1:c.2131-48_2131-38delinsATTTCCTGTCT (SCN9A)	XP_016860158.1:n.2131-48_2131-38delinsATTTCCTGTCT
XR_001738886.1:n.3343-48_3343-38delinsATTTCCTGTCT (SCN9A)