Canonical Allele Identifier: CA2577144832

Gene: SCN9A SCN1A-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166228690_166228691del , CM000664.2:g.166228690_166228691del	GRCh38
NC_000002.11:g.167085200_167085201del , CM000664.1:g.167085200_167085201del	GRCh37
NC_000002.10:g.166793446_166793447del	NCBI36
NG_012798.1:g.152298_152299del , LRG_369:g.152298_152299del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303354.11:c.4206+1_4206+2del (SCN9A)
ENST00000409435.6:c.4206+1_4206+2del (SCN9A)
ENST00000642356.2:c.4206+1_4206+2del (SCN9A)
ENST00000644316.1:c.4050+1_4050+2del (SCN9A)
ENST00000645907.1:c.4173+1_4173+2del (SCN9A)
ENST00000303354.10:c.4206+1_4206+2del (SCN9A)
ENST00000409435.5:c.4206+1_4206+2del (SCN9A)
ENST00000409672.5:c.4173+1_4173+2del (SCN9A)
NM_002977.3:c.4173+1_4173+2del , LRG_369t1:c.4173+1_4173+2del (SCN9A)
NR_110260.1:n.612-19505_612-19504del (SCN1A-AS1)
XM_005246757.1:c.4206+1_4206+2del (SCN9A)
XM_011511616.1:c.4206+1_4206+2del (SCN9A)
XM_011511617.1:c.4206+1_4206+2del (SCN9A)
XM_011511618.1:c.4173+1_4173+2del (SCN9A)
XM_011511619.1:c.4206+1_4206+2del (SCN9A)
NM_001365536.1:c.4206+1_4206+2del (SCN9A)
XM_011511616.3:c.4206+1_4206+2del (SCN9A)
XM_011511617.2:c.4206+1_4206+2del (SCN9A)
XM_011511618.2:c.4173+1_4173+2del (SCN9A)
XM_011511619.2:c.4206+1_4206+2del (SCN9A)
XM_017004668.1:c.3819+1_3819+2del (SCN9A)
XM_017004669.1:c.3462+1_3462+2del (SCN9A)