Canonical Allele Identifier: CA760228393

Gene: SCN9A SCN1A-AS1

Linked Data

• dbSNP Id: rs1205452112
• MyVariant Identifiers: chr2:g.167052156_167052157insC (hg19) ; chr2:g.166195646_166195647insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166195647dup , CM000664.2:g.166195647dup	GRCh38
NC_000002.11:g.167052157dup , CM000664.1:g.167052157dup	GRCh37
NC_000002.10:g.166760403dup	NCBI36
NG_012798.1:g.185341dup , LRG_369:g.185341dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303354.11:c.*3025dup (SCN9A)	ENSP00000304748.7:n.*3025dup
ENST00000642356.2:c.*3025dup (SCN9A) MANE Select	ENSP00000495601.1:n.*3025dup
ENST00000303354.10:c.*3025dup (SCN9A)	ENSP00000304748.7:n.*3025dup
ENST00000409672.5:c.*3025dup (SCN9A)	ENSP00000386306.1:n.*3025dup
NM_002977.3:c.*3025dup , LRG_369t1:c.*3025dup (SCN9A)	NP_002968.1:n.*3025dup
NR_110260.1:n.432-3992dup (SCN1A-AS1)
NM_001365536.1:c.*3025dup (SCN9A) MANE Select	NP_001352465.1:n.*3025dup