Canonical Allele Identifier: CA59810142

Gene: SCN9A SCN1A-AS1

Linked Data

• dbSNP Id: rs759716520
• MyVariant Identifiers: chr2:g.167085141_167085142insTT (hg19) ; chr2:g.166228631_166228632insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166228632_166228633dup , CM000664.2:g.166228632_166228633dup	GRCh38
NC_000002.11:g.167085142_167085143dup , CM000664.1:g.167085142_167085143dup	GRCh37
NC_000002.10:g.166793388_166793389dup	NCBI36
NG_012798.1:g.152355_152356dup , LRG_369:g.152355_152356dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303354.11:c.4206+58_4206+59dup (SCN9A)	ENSP00000304748.7:n.4206+58_4206+59dup
ENST00000409435.6:c.4206+58_4206+59dup (SCN9A)	ENSP00000386330.2:n.4206+58_4206+59dup
ENST00000642356.2:c.4206+58_4206+59dup (SCN9A) MANE Select	ENSP00000495601.1:n.4206+58_4206+59dup
ENST00000644316.1:c.4050+58_4050+59dup (SCN9A)	ENSP00000493939.1:n.4050+58_4050+59dup
ENST00000645907.1:c.4173+58_4173+59dup (SCN9A)	ENSP00000495983.1:n.4173+58_4173+59dup
ENST00000303354.10:c.4206+58_4206+59dup (SCN9A)	ENSP00000304748.7:n.4206+58_4206+59dup
ENST00000409435.5:c.4206+58_4206+59dup (SCN9A)	ENSP00000386330.1:n.4206+58_4206+59dup
ENST00000409672.5:c.4173+58_4173+59dup (SCN9A)	ENSP00000386306.1:n.4173+58_4173+59dup
NM_002977.3:c.4173+58_4173+59dup , LRG_369t1:c.4173+58_4173+59dup (SCN9A)	NP_002968.1:n.4173+58_4173+59dup
NR_110260.1:n.612-19563_612-19562dup (SCN1A-AS1)
XM_005246757.1:c.4206+58_4206+59dup (SCN9A)	XP_005246814.1:n.4206+58_4206+59dup
XM_011511616.1:c.4206+58_4206+59dup (SCN9A)	XP_011509918.1:n.4206+58_4206+59dup
XM_011511617.1:c.4206+58_4206+59dup (SCN9A)	XP_011509919.1:n.4206+58_4206+59dup
XM_011511618.1:c.4173+58_4173+59dup (SCN9A)	XP_011509920.1:n.4173+58_4173+59dup
XM_011511619.1:c.4206+58_4206+59dup (SCN9A)	XP_011509921.1:n.4206+58_4206+59dup
NM_001365536.1:c.4206+58_4206+59dup (SCN9A) MANE Select	NP_001352465.1:n.4206+58_4206+59dup
XM_011511616.3:c.4206+58_4206+59dup (SCN9A)	XP_011509918.1:n.4206+58_4206+59dup
XM_011511617.2:c.4206+58_4206+59dup (SCN9A)	XP_011509919.1:n.4206+58_4206+59dup
XM_011511618.2:c.4173+58_4173+59dup (SCN9A)	XP_011509920.1:n.4173+58_4173+59dup
XM_011511619.2:c.4206+58_4206+59dup (SCN9A)	XP_011509921.1:n.4206+58_4206+59dup
XM_017004668.1:c.3819+58_3819+59dup (SCN9A)	XP_016860157.1:n.3819+58_3819+59dup
XM_017004669.1:c.3462+58_3462+59dup (SCN9A)	XP_016860158.1:n.3462+58_3462+59dup