Canonical Allele Identifier: CA2665121258

Gene: SCN10A

Linked Data

• gnomAD v4: 3-38752124-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38752127del , CM000665.2:g.38752127del	GRCh38
NC_000003.11:g.38793618del , CM000665.1:g.38793618del	GRCh37
NC_000003.10:g.38768622del	NCBI36
NG_031891.2:g.46886del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.1755+94del MANE Select	ENSP00000390600.2:n.1755+94del
ENST00000643924.1:c.1755+94del	ENSP00000495595.1:n.1755+94del
ENST00000655275.1:c.1782+94del	ENSP00000499510.1:n.1782+94del
ENST00000449082.2:c.1755+94del	ENSP00000390600.2:n.1755+94del
NM_001293306.2:c.1755+94del	NP_001280235.2:n.1755+94del
NM_001293307.2:c.1462-1941del	NP_001280236.2:n.1462-1941del
NM_006514.3:c.1755+94del	NP_006505.3:n.1755+94del
XM_005265371.2:c.1764+94del	XP_005265428.1:n.1764+94del
XM_011533993.1:c.1764+94del	XP_011532295.1:n.1764+94del
XM_011533994.1:c.1471-1941del	XP_011532296.1:n.1471-1941del
XM_005265371.3:c.1764+94del	XP_005265428.1:n.1764+94del
XM_011533993.2:c.1764+94del	XP_011532295.1:n.1764+94del
XM_011533994.2:c.1471-1941del	XP_011532296.1:n.1471-1941del
NM_006514.4:c.1755+94del MANE Select	NP_006505.4:n.1755+94del