Canonical Allele Identifier: CA349084773

Gene: SCN9A SCN1A-AS1

Linked Data

• gnomAD v4: 2-166286512-T-C
• MyVariant Identifiers: chr2:g.167143022T>C (hg19) ; chr2:g.166286512T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166286512T>C , CM000664.2:g.166286512T>C	GRCh38
NC_000002.11:g.167143022T>C , CM000664.1:g.167143022T>C	GRCh37
NC_000002.10:g.166851268T>C	NCBI36
NG_012798.1:g.94476A>G , LRG_369:g.94476A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000303354.11:c.1426A>G (SCN9A)	ENSP00000304748.7:p.Arg476Gly
ENST00000409435.6:c.1426A>G (SCN9A)	ENSP00000386330.2:p.Arg476Gly
ENST00000454569.6:c.1426A>G (SCN9A)	ENSP00000413212.2:p.Arg476Gly
ENST00000642356.2:c.1426A>G (SCN9A) MANE Select	ENSP00000495601.1:p.Arg476Gly
ENST00000644316.1:c.1426A>G (SCN9A)	ENSP00000493939.1:p.Arg476Gly
ENST00000645907.1:c.1426A>G (SCN9A)	ENSP00000495983.1:p.Arg476Gly
ENST00000667201.2:c.461A>G (SCN9A)
ENST00000303354.10:c.1426A>G (SCN9A)	ENSP00000304748.7:p.Arg476Gly
ENST00000409435.5:c.1426A>G (SCN9A)	ENSP00000386330.1:p.Arg476Gly
ENST00000409672.5:c.1426A>G (SCN9A)	ENSP00000386306.1:p.Arg476Gly
ENST00000452182.1:c.1021A>G (SCN9A)	ENSP00000393141.1:p.Arg341Gly
ENST00000454569.5:c.1021A>G (SCN9A)	ENSP00000413212.1:p.Arg341Gly
NM_002977.3:c.1426A>G , LRG_369t1:c.1426A>G (SCN9A)	NP_002968.1:p.Arg476Gly
NR_110260.1:n.1030-8053T>C (SCN1A-AS1)
XM_005246757.1:c.1426A>G (SCN9A)	XP_005246814.1:p.Arg476Gly
XM_011511616.1:c.1426A>G (SCN9A)	XP_011509918.1:p.Arg476Gly
XM_011511617.1:c.1426A>G (SCN9A)	XP_011509919.1:p.Arg476Gly
XM_011511618.1:c.1426A>G (SCN9A)	XP_011509920.1:p.Arg476Gly
XM_011511619.1:c.1426A>G (SCN9A)	XP_011509921.1:p.Arg476Gly
NM_001365536.1:c.1426A>G (SCN9A) MANE Select	NP_001352465.1:p.Arg476Gly
XM_011511616.3:c.1426A>G (SCN9A)	XP_011509918.1:p.Arg476Gly
XM_011511617.2:c.1426A>G (SCN9A)	XP_011509919.1:p.Arg476Gly
XM_011511618.2:c.1426A>G (SCN9A)	XP_011509920.1:p.Arg476Gly
XM_011511619.2:c.1426A>G (SCN9A)	XP_011509921.1:p.Arg476Gly
XM_017004668.1:c.1039A>G (SCN9A)	XP_016860157.1:p.Arg347Gly
XM_017004669.1:c.682A>G (SCN9A)	XP_016860158.1:p.Arg228Gly
XR_001738886.1:n.1740A>G (SCN9A)