Canonical Allele Identifier: CA916700893
Gene: SCN9A HGNC NCBI
SCN1A-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1553472237

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166196050_166196060del , CM000664.2:g.166196050_166196060del GRCh38
NC_000002.11:g.167052560_167052570del , CM000664.1:g.167052560_167052570del GRCh37
NC_000002.10:g.166760806_166760816del NCBI36
NG_012798.1:g.184929_184939del , LRG_369:g.184929_184939del

Transcript Alleles

HGVS Amino-acid change
ENST00000303354.11:c.*2613_*2623del (SCN9A) ENSP00000304748.7:n.*2613_*2623del
ENST00000642356.2:c.*2613_*2623del (SCN9A) MANE Select ENSP00000495601.1:n.*2613_*2623del
ENST00000303354.10:c.*2613_*2623del (SCN9A) ENSP00000304748.7:n.*2613_*2623del
ENST00000409672.5:c.*2613_*2623del (SCN9A) ENSP00000386306.1:n.*2613_*2623del
NM_002977.3:c.*2613_*2623del , LRG_369t1:c.*2613_*2623del (SCN9A) NP_002968.1:n.*2613_*2623del
NR_110260.1:n.432-3589_432-3579del (SCN1A-AS1)
NM_001365536.1:c.*2613_*2623del (SCN9A) MANE Select NP_001352465.1:n.*2613_*2623del