Canonical Allele Identifier: CA349091583

Gene: SCN9A

Linked Data

• MyVariant Identifiers: chr2:g.167159598A>C (hg19) ; chr2:g.166303088A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166303088A>C , CM000664.2:g.166303088A>C	GRCh38
NC_000002.11:g.167159598A>C , CM000664.1:g.167159598A>C	GRCh37
NC_000002.10:g.166867844A>C	NCBI36
NG_012798.1:g.77900T>G , LRG_369:g.77900T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000303354.11:c.901+2T>G	ENSP00000304748.7:n.901+2T>G
ENST00000409435.6:c.901+2T>G	ENSP00000386330.2:n.901+2T>G
ENST00000452182.2:c.901+2T>G	ENSP00000393141.2:n.901+2T>G
ENST00000454569.6:c.901+2T>G	ENSP00000413212.2:n.901+2T>G
ENST00000472119.2:n.1258T>G
ENST00000642356.2:c.901+2T>G MANE Select	ENSP00000495601.1:n.901+2T>G
ENST00000644316.1:c.901+2T>G	ENSP00000493939.1:n.901+2T>G
ENST00000645815.1:n.274T>G
ENST00000645907.1:c.901+2T>G	ENSP00000495983.1:n.901+2T>G
ENST00000303354.10:c.901+2T>G	ENSP00000304748.7:n.901+2T>G
ENST00000409435.5:c.901+2T>G	ENSP00000386330.1:n.901+2T>G
ENST00000409672.5:c.901+2T>G	ENSP00000386306.1:n.901+2T>G
ENST00000452182.1:c.496+2T>G	ENSP00000393141.1:n.496+2T>G
ENST00000454569.5:c.496+2T>G	ENSP00000413212.1:n.496+2T>G
ENST00000472119.1:n.436T>G
NM_002977.3:c.901+2T>G , LRG_369t1:c.901+2T>G	NP_002968.1:n.901+2T>G
XM_005246757.1:c.901+2T>G	XP_005246814.1:n.901+2T>G
XM_011511616.1:c.901+2T>G	XP_011509918.1:n.901+2T>G
XM_011511617.1:c.901+2T>G	XP_011509919.1:n.901+2T>G
XM_011511618.1:c.901+2T>G	XP_011509920.1:n.901+2T>G
XM_011511619.1:c.901+2T>G	XP_011509921.1:n.901+2T>G
NM_001365536.1:c.901+2T>G MANE Select	NP_001352465.1:n.901+2T>G
XM_011511616.3:c.901+2T>G	XP_011509918.1:n.901+2T>G
XM_011511617.2:c.901+2T>G	XP_011509919.1:n.901+2T>G
XM_011511618.2:c.901+2T>G	XP_011509920.1:n.901+2T>G
XM_011511619.2:c.901+2T>G	XP_011509921.1:n.901+2T>G
XM_017004668.1:c.514+2T>G	XP_016860157.1:n.514+2T>G
XM_017004669.1:c.157+2T>G	XP_016860158.1:n.157+2T>G
XR_001738886.1:n.1215+2T>G