Canonical Allele Identifier: CA906865079

Gene: SCN10A

Linked Data

• dbSNP Id: rs1160400049
• gnomAD v3: 3-38725116-GC-G
• gnomAD v4: 3-38725116-GC-G
• MyVariant Identifiers: chr3:g.38766608del (hg19) ; chr3:g.38725117del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725119del , CM000665.2:g.38725119del	GRCh38
NC_000003.11:g.38766610del , CM000665.1:g.38766610del	GRCh37
NC_000003.10:g.38741614del	NCBI36
NG_031891.2:g.73894del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3228+57del MANE Select	ENSP00000390600.2:n.3228+57del
ENST00000643924.1:c.3225+57del	ENSP00000495595.1:n.3225+57del
ENST00000655275.1:c.3252+57del	ENSP00000499510.1:n.3252+57del
ENST00000449082.2:c.3228+57del	ENSP00000390600.2:n.3228+57del
NM_001293306.2:c.3225+57del	NP_001280235.2:n.3225+57del
NM_001293307.2:c.2934+57del	NP_001280236.2:n.2934+57del
NM_006514.3:c.3228+57del	NP_006505.3:n.3228+57del
XM_005265371.2:c.3237+57del	XP_005265428.1:n.3237+57del
XM_011533993.1:c.3234+57del	XP_011532295.1:n.3234+57del
XM_011533994.1:c.2943+57del	XP_011532296.1:n.2943+57del
XM_005265371.3:c.3237+57del	XP_005265428.1:n.3237+57del
XM_011533993.2:c.3234+57del	XP_011532295.1:n.3234+57del
XM_011533994.2:c.2943+57del	XP_011532296.1:n.2943+57del
NM_006514.4:c.3228+57del MANE Select	NP_006505.4:n.3228+57del