Canonical Allele Identifier: CA1304976620

Gene: SCN9A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166303520_166303521delinsAG , CM000664.2:g.166303520_166303521delinsAG	GRCh38
NC_000002.11:g.167160030_167160031delinsAG , CM000664.1:g.167160030_167160031delinsAG	GRCh37
NC_000002.10:g.166868276_166868277delinsAG	NCBI36
NG_012798.1:g.77467_77468delinsCT , LRG_369:g.77467_77468delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303354.11:c.689-219_689-218delinsCT	ENSP00000304748.7:n.689-219_689-218delinsCT
ENST00000409435.6:c.689-219_689-218delinsCT	ENSP00000386330.2:n.689-219_689-218delinsCT
ENST00000452182.2:c.689-219_689-218delinsCT	ENSP00000393141.2:n.689-219_689-218delinsCT
ENST00000454569.6:c.689-219_689-218delinsCT	ENSP00000413212.2:n.689-219_689-218delinsCT
ENST00000472119.2:n.1044-219_1044-218delinsCT
ENST00000642356.2:c.689-219_689-218delinsCT MANE Select	ENSP00000495601.1:n.689-219_689-218delinsCT
ENST00000644316.1:c.689-219_689-218delinsCT	ENSP00000493939.1:n.689-219_689-218delinsCT
ENST00000645815.1:n.60-219_60-218delinsCT
ENST00000645907.1:c.689-219_689-218delinsCT	ENSP00000495983.1:n.689-219_689-218delinsCT
ENST00000303354.10:c.689-219_689-218delinsCT	ENSP00000304748.7:n.689-219_689-218delinsCT
ENST00000409435.5:c.689-219_689-218delinsCT	ENSP00000386330.1:n.689-219_689-218delinsCT
ENST00000409672.5:c.689-219_689-218delinsCT	ENSP00000386306.1:n.689-219_689-218delinsCT
ENST00000452182.1:c.284-219_284-218delinsCT	ENSP00000393141.1:n.284-219_284-218delinsCT
ENST00000454569.5:c.284-219_284-218delinsCT	ENSP00000413212.1:n.284-219_284-218delinsCT
ENST00000472119.1:n.222-219_222-218delinsCT
NM_002977.3:c.689-219_689-218delinsCT , LRG_369t1:c.689-219_689-218delinsCT	NP_002968.1:n.689-219_689-218delinsCT
XM_005246757.1:c.689-219_689-218delinsCT	XP_005246814.1:n.689-219_689-218delinsCT
XM_011511616.1:c.689-219_689-218delinsCT	XP_011509918.1:n.689-219_689-218delinsCT
XM_011511617.1:c.689-219_689-218delinsCT	XP_011509919.1:n.689-219_689-218delinsCT
XM_011511618.1:c.689-219_689-218delinsCT	XP_011509920.1:n.689-219_689-218delinsCT
XM_011511619.1:c.689-219_689-218delinsCT	XP_011509921.1:n.689-219_689-218delinsCT
NM_001365536.1:c.689-219_689-218delinsCT MANE Select	NP_001352465.1:n.689-219_689-218delinsCT
XM_011511616.3:c.689-219_689-218delinsCT	XP_011509918.1:n.689-219_689-218delinsCT
XM_011511617.2:c.689-219_689-218delinsCT	XP_011509919.1:n.689-219_689-218delinsCT
XM_011511618.2:c.689-219_689-218delinsCT	XP_011509920.1:n.689-219_689-218delinsCT
XM_011511619.2:c.689-219_689-218delinsCT	XP_011509921.1:n.689-219_689-218delinsCT
XM_017004668.1:c.302-219_302-218delinsCT	XP_016860157.1:n.302-219_302-218delinsCT
XM_017004669.1:c.-56-219_-56-218delinsCT	XP_016860158.1:n.-56-219_-56-218delinsCT
XR_001738886.1:n.1003-219_1003-218delinsCT