Canonical Allele Identifier: CA349074025

Gene: SCN9A SCN1A-AS1

Linked Data

• dbSNP Id: rs1305266156
• MyVariant Identifiers: chr2:g.167129184G>A (hg19) ; chr2:g.166272674G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166272674G>A , CM000664.2:g.166272674G>A	GRCh38
NC_000002.11:g.167129184G>A , CM000664.1:g.167129184G>A	GRCh37
NC_000002.10:g.166837430G>A	NCBI36
NG_012798.1:g.108314C>T , LRG_369:g.108314C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303354.11:c.3076C>T (SCN9A)	ENSP00000304748.7:p.Gln1026Ter
ENST00000409435.6:c.3076C>T (SCN9A)	ENSP00000386330.2:p.Gln1026Ter
ENST00000642356.2:c.3076C>T (SCN9A) MANE Select	ENSP00000495601.1:p.Gln1026Ter
ENST00000643319.1:c.76C>T (SCN9A)	ENSP00000494071.1:p.Gln26Ter
ENST00000644316.1:c.3043C>T (SCN9A)	ENSP00000493939.1:p.Gln1015Ter
ENST00000645907.1:c.3043C>T (SCN9A)	ENSP00000495983.1:p.Gln1015Ter
ENST00000667201.2:c.1877-176C>T (SCN9A)
ENST00000303354.10:c.3076C>T (SCN9A)	ENSP00000304748.7:p.Gln1026Ter
ENST00000409435.5:c.3076C>T (SCN9A)	ENSP00000386330.1:p.Gln1026Ter
ENST00000409672.5:c.3043C>T (SCN9A)	ENSP00000386306.1:p.Gln1015Ter
NM_002977.3:c.3043C>T , LRG_369t1:c.3043C>T (SCN9A)	NP_002968.1:p.Gln1015Ter
NR_110260.1:n.870-4414G>A (SCN1A-AS1)
XM_005246757.1:c.3076C>T (SCN9A)	XP_005246814.1:p.Gln1026Ter
XM_011511616.1:c.3076C>T (SCN9A)	XP_011509918.1:p.Gln1026Ter
XM_011511617.1:c.3076C>T (SCN9A)	XP_011509919.1:p.Gln1026Ter
XM_011511618.1:c.3043C>T (SCN9A)	XP_011509920.1:p.Gln1015Ter
XM_011511619.1:c.3076C>T (SCN9A)	XP_011509921.1:p.Gln1026Ter
NM_001365536.1:c.3076C>T (SCN9A) MANE Select	NP_001352465.1:p.Gln1026Ter
XM_011511616.3:c.3076C>T (SCN9A)	XP_011509918.1:p.Gln1026Ter
XM_011511617.2:c.3076C>T (SCN9A)	XP_011509919.1:p.Gln1026Ter
XM_011511618.2:c.3043C>T (SCN9A)	XP_011509920.1:p.Gln1015Ter
XM_011511619.2:c.3076C>T (SCN9A)	XP_011509921.1:p.Gln1026Ter
XM_017004668.1:c.2689C>T (SCN9A)	XP_016860157.1:p.Gln897Ter
XM_017004669.1:c.2332C>T (SCN9A)	XP_016860158.1:p.Gln778Ter