Canonical Allele Identifier: CA2661765550

Gene: SCN9A SCN1A-AS1

Linked Data

• gnomAD v4: 2-166233201-G-GGA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166233201_166233202insGA , CM000664.2:g.166233201_166233202insGA	GRCh38
NC_000002.11:g.167089711_167089712insGA , CM000664.1:g.167089711_167089712insGA	GRCh37
NC_000002.10:g.166797957_166797958insGA	NCBI36
NG_012798.1:g.147786_147787insTC , LRG_369:g.147786_147787insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303354.11:c.3924+138_3924+139insTC (SCN9A)	ENSP00000304748.7:n.3924+138_3924+139insTC
ENST00000409435.6:c.3924+138_3924+139insTC (SCN9A)	ENSP00000386330.2:n.3924+138_3924+139insTC
ENST00000642356.2:c.3924+138_3924+139insTC (SCN9A) MANE Select	ENSP00000495601.1:n.3924+138_3924+139insTC
ENST00000644316.1:c.3769-4230_3769-4229insTC (SCN9A)	ENSP00000493939.1:n.3769-4230_3769-4229insTC
ENST00000645907.1:c.3891+138_3891+139insTC (SCN9A)	ENSP00000495983.1:n.3891+138_3891+139insTC
ENST00000303354.10:c.3924+138_3924+139insTC (SCN9A)	ENSP00000304748.7:n.3924+138_3924+139insTC
ENST00000409435.5:c.3924+138_3924+139insTC (SCN9A)	ENSP00000386330.1:n.3924+138_3924+139insTC
ENST00000409672.5:c.3891+138_3891+139insTC (SCN9A)	ENSP00000386306.1:n.3891+138_3891+139insTC
NM_002977.3:c.3891+138_3891+139insTC , LRG_369t1:c.3891+138_3891+139insTC (SCN9A)	NP_002968.1:n.3891+138_3891+139insTC
NR_110260.1:n.612-14994_612-14993insGA (SCN1A-AS1)
XM_005246757.1:c.3924+138_3924+139insTC (SCN9A)	XP_005246814.1:n.3924+138_3924+139insTC
XM_011511616.1:c.3924+138_3924+139insTC (SCN9A)	XP_011509918.1:n.3924+138_3924+139insTC
XM_011511617.1:c.3924+138_3924+139insTC (SCN9A)	XP_011509919.1:n.3924+138_3924+139insTC
XM_011511618.1:c.3891+138_3891+139insTC (SCN9A)	XP_011509920.1:n.3891+138_3891+139insTC
XM_011511619.1:c.3924+138_3924+139insTC (SCN9A)	XP_011509921.1:n.3924+138_3924+139insTC
NM_001365536.1:c.3924+138_3924+139insTC (SCN9A) MANE Select	NP_001352465.1:n.3924+138_3924+139insTC
XM_011511616.3:c.3924+138_3924+139insTC (SCN9A)	XP_011509918.1:n.3924+138_3924+139insTC
XM_011511617.2:c.3924+138_3924+139insTC (SCN9A)	XP_011509919.1:n.3924+138_3924+139insTC
XM_011511618.2:c.3891+138_3891+139insTC (SCN9A)	XP_011509920.1:n.3891+138_3891+139insTC
XM_011511619.2:c.3924+138_3924+139insTC (SCN9A)	XP_011509921.1:n.3924+138_3924+139insTC
XM_017004668.1:c.3537+138_3537+139insTC (SCN9A)	XP_016860157.1:n.3537+138_3537+139insTC
XM_017004669.1:c.3180+138_3180+139insTC (SCN9A)	XP_016860158.1:n.3180+138_3180+139insTC