Canonical Allele Identifier: CA537526007

Gene: SCN9A SCN1A-AS1

Linked Data

• dbSNP Id: rs1392625653
• gnomAD v2: 2-167144631-ACACACACATT-A
• gnomAD v3: 2-166288121-ACACACACATT-A
• gnomAD v4: 2-166288121-ACACACACATT-A
• MyVariant Identifiers: chr2:g.167144632_167144641del (hg19) ; chr2:g.166288122_166288131del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166288122_166288131del , CM000664.2:g.166288122_166288131del	GRCh38
NC_000002.11:g.167144632_167144641del , CM000664.1:g.167144632_167144641del	GRCh37
NC_000002.10:g.166852878_166852887del	NCBI36
NG_012798.1:g.92857_92866del , LRG_369:g.92857_92866del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303354.11:c.1314+306_1314+315del (SCN9A)	ENSP00000304748.7:n.1314+306_1314+315del
ENST00000409435.6:c.1314+306_1314+315del (SCN9A)	ENSP00000386330.2:n.1314+306_1314+315del
ENST00000454569.6:c.1314+306_1314+315del (SCN9A)	ENSP00000413212.2:n.1314+306_1314+315del
ENST00000642356.2:c.1314+306_1314+315del (SCN9A) MANE Select	ENSP00000495601.1:n.1314+306_1314+315del
ENST00000644316.1:c.1314+306_1314+315del (SCN9A)	ENSP00000493939.1:n.1314+306_1314+315del
ENST00000645907.1:c.1314+306_1314+315del (SCN9A)	ENSP00000495983.1:n.1314+306_1314+315del
ENST00000667201.2:c.349+306_349+315del (SCN9A)
ENST00000303354.10:c.1314+306_1314+315del (SCN9A)	ENSP00000304748.7:n.1314+306_1314+315del
ENST00000409435.5:c.1314+306_1314+315del (SCN9A)	ENSP00000386330.1:n.1314+306_1314+315del
ENST00000409672.5:c.1314+306_1314+315del (SCN9A)	ENSP00000386306.1:n.1314+306_1314+315del
ENST00000452182.1:c.909+306_909+315del (SCN9A)	ENSP00000393141.1:n.909+306_909+315del
ENST00000454569.5:c.909+306_909+315del (SCN9A)	ENSP00000413212.1:n.909+306_909+315del
NM_002977.3:c.1314+306_1314+315del , LRG_369t1:c.1314+306_1314+315del (SCN9A)	NP_002968.1:n.1314+306_1314+315del
NR_110260.1:n.1030-6443_1030-6434del (SCN1A-AS1)
XM_005246757.1:c.1314+306_1314+315del (SCN9A)	XP_005246814.1:n.1314+306_1314+315del
XM_011511616.1:c.1314+306_1314+315del (SCN9A)	XP_011509918.1:n.1314+306_1314+315del
XM_011511617.1:c.1314+306_1314+315del (SCN9A)	XP_011509919.1:n.1314+306_1314+315del
XM_011511618.1:c.1314+306_1314+315del (SCN9A)	XP_011509920.1:n.1314+306_1314+315del
XM_011511619.1:c.1314+306_1314+315del (SCN9A)	XP_011509921.1:n.1314+306_1314+315del
NM_001365536.1:c.1314+306_1314+315del (SCN9A) MANE Select	NP_001352465.1:n.1314+306_1314+315del
XM_011511616.3:c.1314+306_1314+315del (SCN9A)	XP_011509918.1:n.1314+306_1314+315del
XM_011511617.2:c.1314+306_1314+315del (SCN9A)	XP_011509919.1:n.1314+306_1314+315del
XM_011511618.2:c.1314+306_1314+315del (SCN9A)	XP_011509920.1:n.1314+306_1314+315del
XM_011511619.2:c.1314+306_1314+315del (SCN9A)	XP_011509921.1:n.1314+306_1314+315del
XM_017004668.1:c.927+306_927+315del (SCN9A)	XP_016860157.1:n.927+306_927+315del
XM_017004669.1:c.570+306_570+315del (SCN9A)	XP_016860158.1:n.570+306_570+315del
XR_001738886.1:n.1628+306_1628+315del (SCN9A)