Canonical Allele Identifier: CA1038852304
Gene: SCN9A HGNC NCBI
SCN1A-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1693248045

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166196368_166196371del , CM000664.2:g.166196368_166196371del GRCh38
NC_000002.11:g.167052878_167052881del , CM000664.1:g.167052878_167052881del GRCh37
NC_000002.10:g.166761124_166761127del NCBI36
NG_012798.1:g.184618_184621del , LRG_369:g.184618_184621del

Transcript Alleles

HGVS Amino-acid change
ENST00000303354.11:c.*2302_*2305del (SCN9A) ENSP00000304748.7:n.*2302_*2305del
ENST00000642356.2:c.*2302_*2305del (SCN9A) MANE Select ENSP00000495601.1:n.*2302_*2305del
ENST00000303354.10:c.*2302_*2305del (SCN9A) ENSP00000304748.7:n.*2302_*2305del
ENST00000409672.5:c.*2302_*2305del (SCN9A) ENSP00000386306.1:n.*2302_*2305del
NM_002977.3:c.*2302_*2305del , LRG_369t1:c.*2302_*2305del (SCN9A) NP_002968.1:n.*2302_*2305del
NR_110260.1:n.432-3271_432-3268del (SCN1A-AS1)
NM_001365536.1:c.*2302_*2305del (SCN9A) MANE Select NP_001352465.1:n.*2302_*2305del