Canonical Allele Identifier: CA59789414

Gene: SCN9A SCN1A-AS1

Linked Data

• dbSNP Id: rs892066112
• gnomAD v3: 2-166204347-T-A
• gnomAD v4: 2-166204347-T-A
• MyVariant Identifiers: chr2:g.167060857T>A (hg19) ; chr2:g.166204347T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166204347T>A , CM000664.2:g.166204347T>A	GRCh38
NC_000002.11:g.167060857T>A , CM000664.1:g.167060857T>A	GRCh37
NC_000002.10:g.166769103T>A	NCBI36
NG_012798.1:g.176641A>T , LRG_369:g.176641A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303354.11:c.4503+13A>T (SCN9A)	ENSP00000304748.7:n.4503+13A>T
ENST00000409435.6:c.4503+13A>T (SCN9A)	ENSP00000386330.2:n.4503+13A>T
ENST00000642356.2:c.4503+13A>T (SCN9A) MANE Select	ENSP00000495601.1:n.4503+13A>T
ENST00000644316.1:c.4347+13A>T (SCN9A)	ENSP00000493939.1:n.4347+13A>T
ENST00000645907.1:c.4470+13A>T (SCN9A)	ENSP00000495983.1:n.4470+13A>T
ENST00000646694.1:n.880+13A>T (SCN9A)
ENST00000303354.10:c.4503+13A>T (SCN9A)	ENSP00000304748.7:n.4503+13A>T
ENST00000409435.5:c.4503+13A>T (SCN9A)	ENSP00000386330.1:n.4503+13A>T
ENST00000409672.5:c.4470+13A>T (SCN9A)	ENSP00000386306.1:n.4470+13A>T
NM_002977.3:c.4470+13A>T , LRG_369t1:c.4470+13A>T (SCN9A)	NP_002968.1:n.4470+13A>T
NR_110260.1:n.611+4529T>A (SCN1A-AS1)
XM_005246757.1:c.4503+13A>T (SCN9A)	XP_005246814.1:n.4503+13A>T
XM_011511616.1:c.4503+13A>T (SCN9A)	XP_011509918.1:n.4503+13A>T
XM_011511617.1:c.4503+13A>T (SCN9A)	XP_011509919.1:n.4503+13A>T
XM_011511618.1:c.4470+13A>T (SCN9A)	XP_011509920.1:n.4470+13A>T
XM_011511619.1:c.4503+13A>T (SCN9A)	XP_011509921.1:n.4503+13A>T
NM_001365536.1:c.4503+13A>T (SCN9A) MANE Select	NP_001352465.1:n.4503+13A>T
XM_011511616.3:c.4503+13A>T (SCN9A)	XP_011509918.1:n.4503+13A>T
XM_011511617.2:c.4503+13A>T (SCN9A)	XP_011509919.1:n.4503+13A>T
XM_011511618.2:c.4470+13A>T (SCN9A)	XP_011509920.1:n.4470+13A>T
XM_011511619.2:c.4503+13A>T (SCN9A)	XP_011509921.1:n.4503+13A>T
XM_017004668.1:c.4116+13A>T (SCN9A)	XP_016860157.1:n.4116+13A>T
XM_017004669.1:c.3759+13A>T (SCN9A)	XP_016860158.1:n.3759+13A>T