Canonical Allele Identifier: CA2539802219

Gene: SCN9A SCN1A-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166288100_166288102del , CM000664.2:g.166288100_166288102del	GRCh38
NC_000002.11:g.167144610_167144612del , CM000664.1:g.167144610_167144612del	GRCh37
NC_000002.10:g.166852856_166852858del	NCBI36
NG_012798.1:g.92886_92888del , LRG_369:g.92886_92888del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303354.11:c.1314+335_1314+337del (SCN9A)	ENSP00000304748.7:n.1314+335_1314+337del
ENST00000409435.6:c.1314+335_1314+337del (SCN9A)	ENSP00000386330.2:n.1314+335_1314+337del
ENST00000454569.6:c.1314+335_1314+337del (SCN9A)	ENSP00000413212.2:n.1314+335_1314+337del
ENST00000642356.2:c.1314+335_1314+337del (SCN9A) MANE Select	ENSP00000495601.1:n.1314+335_1314+337del
ENST00000644316.1:c.1314+335_1314+337del (SCN9A)	ENSP00000493939.1:n.1314+335_1314+337del
ENST00000645907.1:c.1314+335_1314+337del (SCN9A)	ENSP00000495983.1:n.1314+335_1314+337del
ENST00000667201.2:c.349+335_349+337del (SCN9A)
ENST00000303354.10:c.1314+335_1314+337del (SCN9A)	ENSP00000304748.7:n.1314+335_1314+337del
ENST00000409435.5:c.1314+335_1314+337del (SCN9A)	ENSP00000386330.1:n.1314+335_1314+337del
ENST00000409672.5:c.1314+335_1314+337del (SCN9A)	ENSP00000386306.1:n.1314+335_1314+337del
ENST00000452182.1:c.909+335_909+337del (SCN9A)	ENSP00000393141.1:n.909+335_909+337del
ENST00000454569.5:c.909+335_909+337del (SCN9A)	ENSP00000413212.1:n.909+335_909+337del
NM_002977.3:c.1314+335_1314+337del , LRG_369t1:c.1314+335_1314+337del (SCN9A)	NP_002968.1:n.1314+335_1314+337del
NR_110260.1:n.1030-6465_1030-6463del (SCN1A-AS1)
XM_005246757.1:c.1314+335_1314+337del (SCN9A)	XP_005246814.1:n.1314+335_1314+337del
XM_011511616.1:c.1314+335_1314+337del (SCN9A)	XP_011509918.1:n.1314+335_1314+337del
XM_011511617.1:c.1314+335_1314+337del (SCN9A)	XP_011509919.1:n.1314+335_1314+337del
XM_011511618.1:c.1314+335_1314+337del (SCN9A)	XP_011509920.1:n.1314+335_1314+337del
XM_011511619.1:c.1314+335_1314+337del (SCN9A)	XP_011509921.1:n.1314+335_1314+337del
NM_001365536.1:c.1314+335_1314+337del (SCN9A) MANE Select	NP_001352465.1:n.1314+335_1314+337del
XM_011511616.3:c.1314+335_1314+337del (SCN9A)	XP_011509918.1:n.1314+335_1314+337del
XM_011511617.2:c.1314+335_1314+337del (SCN9A)	XP_011509919.1:n.1314+335_1314+337del
XM_011511618.2:c.1314+335_1314+337del (SCN9A)	XP_011509920.1:n.1314+335_1314+337del
XM_011511619.2:c.1314+335_1314+337del (SCN9A)	XP_011509921.1:n.1314+335_1314+337del
XM_017004668.1:c.927+335_927+337del (SCN9A)	XP_016860157.1:n.927+335_927+337del
XM_017004669.1:c.570+335_570+337del (SCN9A)	XP_016860158.1:n.570+335_570+337del
XR_001738886.1:n.1628+335_1628+337del (SCN9A)