Canonical Allele Identifier: CA1304932132

Gene: SCN9A SCN1A-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166204390C= , CM000664.2:g.166204390C=	GRCh38
NC_000002.11:g.167060900C= , CM000664.1:g.167060900C=	GRCh37
NC_000002.10:g.166769146C=	NCBI36
NG_012798.1:g.176598G= , LRG_369:g.176598G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303354.11:c.4473G= (SCN9A)	ENSP00000304748.7:p.Lys1491=
ENST00000409435.6:c.4473G= (SCN9A)	ENSP00000386330.2:p.Lys1491=
ENST00000642356.2:c.4473G= (SCN9A) MANE Select	ENSP00000495601.1:p.Lys1491=
ENST00000644316.1:c.4317G= (SCN9A)	ENSP00000493939.1:p.Lys1439=
ENST00000645907.1:c.4440G= (SCN9A)	ENSP00000495983.1:p.Lys1480=
ENST00000646694.1:n.850G= (SCN9A)
ENST00000303354.10:c.4473G= (SCN9A)	ENSP00000304748.7:p.Lys1491=
ENST00000409435.5:c.4473G= (SCN9A)	ENSP00000386330.1:p.Lys1491=
ENST00000409672.5:c.4440G= (SCN9A)	ENSP00000386306.1:p.Lys1480=
NM_002977.3:c.4440G= , LRG_369t1:c.4440G= (SCN9A)	NP_002968.1:p.Lys1480=
NR_110260.1:n.611+4572C= (SCN1A-AS1)
XM_005246757.1:c.4473G= (SCN9A)	XP_005246814.1:p.Lys1491=
XM_011511616.1:c.4473G= (SCN9A)	XP_011509918.1:p.Lys1491=
XM_011511617.1:c.4473G= (SCN9A)	XP_011509919.1:p.Lys1491=
XM_011511618.1:c.4440G= (SCN9A)	XP_011509920.1:p.Lys1480=
XM_011511619.1:c.4473G= (SCN9A)	XP_011509921.1:p.Lys1491=
NM_001365536.1:c.4473G= (SCN9A) MANE Select	NP_001352465.1:p.Lys1491=
XM_011511616.3:c.4473G= (SCN9A)	XP_011509918.1:p.Lys1491=
XM_011511617.2:c.4473G= (SCN9A)	XP_011509919.1:p.Lys1491=
XM_011511618.2:c.4440G= (SCN9A)	XP_011509920.1:p.Lys1480=
XM_011511619.2:c.4473G= (SCN9A)	XP_011509921.1:p.Lys1491=
XM_017004668.1:c.4086G= (SCN9A)	XP_016860157.1:p.Lys1362=
XM_017004669.1:c.3729G= (SCN9A)	XP_016860158.1:p.Lys1243=