Canonical Allele Identifier: CA349077862

Gene: SCN9A SCN1A-AS1

Linked Data

• MyVariant Identifiers: chr2:g.167133708G>C (hg19) ; chr2:g.166277198G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166277198G>C , CM000664.2:g.166277198G>C	GRCh38
NC_000002.11:g.167133708G>C , CM000664.1:g.167133708G>C	GRCh37
NC_000002.10:g.166841954G>C	NCBI36
NG_012798.1:g.103790C>G , LRG_369:g.103790C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303354.11:c.2659C>G (SCN9A)	ENSP00000304748.7:p.Leu887Val
ENST00000409435.6:c.2659C>G (SCN9A)	ENSP00000386330.2:p.Leu887Val
ENST00000642356.2:c.2659C>G (SCN9A) MANE Select	ENSP00000495601.1:p.Leu887Val
ENST00000644316.1:c.2626C>G (SCN9A)	ENSP00000493939.1:p.Leu876Val
ENST00000645283.1:c.316C>G (SCN9A)	ENSP00000496086.1:p.Leu106Val
ENST00000645907.1:c.2626C>G (SCN9A)	ENSP00000495983.1:p.Leu876Val
ENST00000667201.2:c.1661C>G (SCN9A)
ENST00000303354.10:c.2659C>G (SCN9A)	ENSP00000304748.7:p.Leu887Val
ENST00000409435.5:c.2659C>G (SCN9A)	ENSP00000386330.1:p.Leu887Val
ENST00000409672.5:c.2626C>G (SCN9A)	ENSP00000386306.1:p.Leu876Val
NM_002977.3:c.2626C>G , LRG_369t1:c.2626C>G (SCN9A)	NP_002968.1:p.Leu876Val
NR_110260.1:n.980G>C (SCN1A-AS1)
XM_005246757.1:c.2659C>G (SCN9A)	XP_005246814.1:p.Leu887Val
XM_011511616.1:c.2659C>G (SCN9A)	XP_011509918.1:p.Leu887Val
XM_011511617.1:c.2659C>G (SCN9A)	XP_011509919.1:p.Leu887Val
XM_011511618.1:c.2626C>G (SCN9A)	XP_011509920.1:p.Leu876Val
XM_011511619.1:c.2659C>G (SCN9A)	XP_011509921.1:p.Leu887Val
NM_001365536.1:c.2659C>G (SCN9A) MANE Select	NP_001352465.1:p.Leu887Val
XM_011511616.3:c.2659C>G (SCN9A)	XP_011509918.1:p.Leu887Val
XM_011511617.2:c.2659C>G (SCN9A)	XP_011509919.1:p.Leu887Val
XM_011511618.2:c.2626C>G (SCN9A)	XP_011509920.1:p.Leu876Val
XM_011511619.2:c.2659C>G (SCN9A)	XP_011509921.1:p.Leu887Val
XM_017004668.1:c.2272C>G (SCN9A)	XP_016860157.1:p.Leu758Val
XM_017004669.1:c.1915C>G (SCN9A)	XP_016860158.1:p.Leu639Val
XR_001738886.1:n.2973C>G (SCN9A)