Canonical Allele Identifier: CA1358640854

Gene: SCN10A

Linked Data

• dbSNP Id: rs2063448443

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725850_38725862dup , CM000665.2:g.38725850_38725862dup	GRCh38
NC_000003.11:g.38767341_38767353dup , CM000665.1:g.38767341_38767353dup	GRCh37
NC_000003.10:g.38742345_38742357dup	NCBI36
NG_031891.2:g.73149_73161dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3088-548_3088-536dup MANE Select	ENSP00000390600.2:n.3088-548_3088-536dup
ENST00000643924.1:c.3088-551_3088-539dup	ENSP00000495595.1:n.3088-551_3088-539dup
ENST00000655275.1:c.3115-551_3115-539dup	ENSP00000499510.1:n.3115-551_3115-539dup
ENST00000449082.2:c.3088-548_3088-536dup	ENSP00000390600.2:n.3088-548_3088-536dup
NM_001293306.2:c.3088-551_3088-539dup	NP_001280235.2:n.3088-551_3088-539dup
NM_001293307.2:c.2794-548_2794-536dup	NP_001280236.2:n.2794-548_2794-536dup
NM_006514.3:c.3088-548_3088-536dup	NP_006505.3:n.3088-548_3088-536dup
XM_005265371.2:c.3097-548_3097-536dup	XP_005265428.1:n.3097-548_3097-536dup
XM_011533993.1:c.3097-551_3097-539dup	XP_011532295.1:n.3097-551_3097-539dup
XM_011533994.1:c.2803-548_2803-536dup	XP_011532296.1:n.2803-548_2803-536dup
XM_005265371.3:c.3097-548_3097-536dup	XP_005265428.1:n.3097-548_3097-536dup
XM_011533993.2:c.3097-551_3097-539dup	XP_011532295.1:n.3097-551_3097-539dup
XM_011533994.2:c.2803-548_2803-536dup	XP_011532296.1:n.2803-548_2803-536dup
NM_006514.4:c.3088-548_3088-536dup MANE Select	NP_006505.4:n.3088-548_3088-536dup