Canonical Allele Identifier: CA11403338

Gene: SCN10A

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38723999C>T , CM000665.2:g.38723999C>T	GRCh38
NC_000003.11:g.38765490C>T , CM000665.1:g.38765490C>T	GRCh37
NC_000003.10:g.38740494C>T	NCBI36
NG_031891.2:g.75012G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3229-446G>A MANE Select	ENSP00000390600.2:n.3229-446G>A
ENST00000643924.1:c.3226-446G>A	ENSP00000495595.1:n.3226-446G>A
ENST00000655275.1:c.3253-446G>A	ENSP00000499510.1:n.3253-446G>A
ENST00000449082.2:c.3229-446G>A	ENSP00000390600.2:n.3229-446G>A
NM_001293306.2:c.3226-446G>A	NP_001280235.2:n.3226-446G>A
NM_001293307.2:c.2935-446G>A	NP_001280236.2:n.2935-446G>A
NM_006514.3:c.3229-446G>A	NP_006505.3:n.3229-446G>A
XM_005265371.2:c.3238-446G>A	XP_005265428.1:n.3238-446G>A
XM_011533993.1:c.3235-446G>A	XP_011532295.1:n.3235-446G>A
XM_011533994.1:c.2944-446G>A	XP_011532296.1:n.2944-446G>A
XM_005265371.3:c.3238-446G>A	XP_005265428.1:n.3238-446G>A
XM_011533993.2:c.3235-446G>A	XP_011532295.1:n.3235-446G>A
XM_011533994.2:c.2944-446G>A	XP_011532296.1:n.2944-446G>A
NM_006514.4:c.3229-446G>A MANE Select	NP_006505.4:n.3229-446G>A