Canonical Allele Identifier: CA349070278

Gene: SCN9A SCN1A-AS1

Linked Data

• MyVariant Identifiers: chr2:g.167099073A>T (hg19) ; chr2:g.166242563A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166242563A>T , CM000664.2:g.166242563A>T	GRCh38
NC_000002.11:g.167099073A>T , CM000664.1:g.167099073A>T	GRCh37
NC_000002.10:g.166807319A>T	NCBI36
NG_012798.1:g.138425T>A , LRG_369:g.138425T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000303354.11:c.3566T>A (SCN9A)	ENSP00000304748.7:p.Val1189Asp
ENST00000409435.6:c.3566T>A (SCN9A)	ENSP00000386330.2:p.Val1189Asp
ENST00000642356.2:c.3566T>A (SCN9A) MANE Select	ENSP00000495601.1:p.Val1189Asp
ENST00000644316.1:c.3533T>A (SCN9A)	ENSP00000493939.1:p.Val1178Asp
ENST00000645907.1:c.3533T>A (SCN9A)	ENSP00000495983.1:p.Val1178Asp
ENST00000303354.10:c.3566T>A (SCN9A)	ENSP00000304748.7:p.Val1189Asp
ENST00000409435.5:c.3566T>A (SCN9A)	ENSP00000386330.1:p.Val1189Asp
ENST00000409672.5:c.3533T>A (SCN9A)	ENSP00000386306.1:p.Val1178Asp
NM_002977.3:c.3533T>A , LRG_369t1:c.3533T>A (SCN9A)	NP_002968.1:p.Val1178Asp
NR_110260.1:n.612-5632A>T (SCN1A-AS1)
XM_005246757.1:c.3566T>A (SCN9A)	XP_005246814.1:p.Val1189Asp
XM_011511616.1:c.3566T>A (SCN9A)	XP_011509918.1:p.Val1189Asp
XM_011511617.1:c.3566T>A (SCN9A)	XP_011509919.1:p.Val1189Asp
XM_011511618.1:c.3533T>A (SCN9A)	XP_011509920.1:p.Val1178Asp
XM_011511619.1:c.3566T>A (SCN9A)	XP_011509921.1:p.Val1189Asp
NM_001365536.1:c.3566T>A (SCN9A) MANE Select	NP_001352465.1:p.Val1189Asp
XM_011511616.3:c.3566T>A (SCN9A)	XP_011509918.1:p.Val1189Asp
XM_011511617.2:c.3566T>A (SCN9A)	XP_011509919.1:p.Val1189Asp
XM_011511618.2:c.3533T>A (SCN9A)	XP_011509920.1:p.Val1178Asp
XM_011511619.2:c.3566T>A (SCN9A)	XP_011509921.1:p.Val1189Asp
XM_017004668.1:c.3179T>A (SCN9A)	XP_016860157.1:p.Val1060Asp
XM_017004669.1:c.2822T>A (SCN9A)	XP_016860158.1:p.Val941Asp