Canonical Allele Identifier: CA349077774

Gene: SCN9A SCN1A-AS1

Linked Data

• MyVariant Identifiers: chr2:g.167133671A>G (hg19) ; chr2:g.166277161A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166277161A>G , CM000664.2:g.166277161A>G	GRCh38
NC_000002.11:g.167133671A>G , CM000664.1:g.167133671A>G	GRCh37
NC_000002.10:g.166841917A>G	NCBI36
NG_012798.1:g.103827T>C , LRG_369:g.103827T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303354.11:c.2696T>C (SCN9A)	ENSP00000304748.7:p.Ile899Thr
ENST00000409435.6:c.2696T>C (SCN9A)	ENSP00000386330.2:p.Ile899Thr
ENST00000642356.2:c.2696T>C (SCN9A) MANE Select	ENSP00000495601.1:p.Ile899Thr
ENST00000644316.1:c.2663T>C (SCN9A)	ENSP00000493939.1:p.Ile888Thr
ENST00000645283.1:c.353T>C (SCN9A)	ENSP00000496086.1:p.Ile118Thr
ENST00000645907.1:c.2663T>C (SCN9A)	ENSP00000495983.1:p.Ile888Thr
ENST00000667201.2:c.1698T>C (SCN9A)
ENST00000303354.10:c.2696T>C (SCN9A)	ENSP00000304748.7:p.Ile899Thr
ENST00000409435.5:c.2696T>C (SCN9A)	ENSP00000386330.1:p.Ile899Thr
ENST00000409672.5:c.2663T>C (SCN9A)	ENSP00000386306.1:p.Ile888Thr
NM_002977.3:c.2663T>C , LRG_369t1:c.2663T>C (SCN9A)	NP_002968.1:p.Ile888Thr
NR_110260.1:n.943A>G (SCN1A-AS1)
XM_005246757.1:c.2696T>C (SCN9A)	XP_005246814.1:p.Ile899Thr
XM_011511616.1:c.2696T>C (SCN9A)	XP_011509918.1:p.Ile899Thr
XM_011511617.1:c.2696T>C (SCN9A)	XP_011509919.1:p.Ile899Thr
XM_011511618.1:c.2663T>C (SCN9A)	XP_011509920.1:p.Ile888Thr
XM_011511619.1:c.2696T>C (SCN9A)	XP_011509921.1:p.Ile899Thr
NM_001365536.1:c.2696T>C (SCN9A) MANE Select	NP_001352465.1:p.Ile899Thr
XM_011511616.3:c.2696T>C (SCN9A)	XP_011509918.1:p.Ile899Thr
XM_011511617.2:c.2696T>C (SCN9A)	XP_011509919.1:p.Ile899Thr
XM_011511618.2:c.2663T>C (SCN9A)	XP_011509920.1:p.Ile888Thr
XM_011511619.2:c.2696T>C (SCN9A)	XP_011509921.1:p.Ile899Thr
XM_017004668.1:c.2309T>C (SCN9A)	XP_016860157.1:p.Ile770Thr
XM_017004669.1:c.1952T>C (SCN9A)	XP_016860158.1:p.Ile651Thr
XR_001738886.1:n.3010T>C (SCN9A)