Canonical Allele Identifier: CA542279032

Gene: SCN10A

Linked Data

• dbSNP Id: rs1417731343
• gnomAD v2: 3-38766443-C-G
• gnomAD v3: 3-38724952-C-G
• gnomAD v4: 3-38724952-C-G
• MyVariant Identifiers: chr3:g.38766443C>G (hg19) ; chr3:g.38724952C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38724952C>G , CM000665.2:g.38724952C>G	GRCh38
NC_000003.11:g.38766443C>G , CM000665.1:g.38766443C>G	GRCh37
NC_000003.10:g.38741447C>G	NCBI36
NG_031891.2:g.74059G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3228+222G>C MANE Select	ENSP00000390600.2:n.3228+222G>C
ENST00000643924.1:c.3225+222G>C	ENSP00000495595.1:n.3225+222G>C
ENST00000655275.1:c.3252+222G>C	ENSP00000499510.1:n.3252+222G>C
ENST00000449082.2:c.3228+222G>C	ENSP00000390600.2:n.3228+222G>C
NM_001293306.2:c.3225+222G>C	NP_001280235.2:n.3225+222G>C
NM_001293307.2:c.2934+222G>C	NP_001280236.2:n.2934+222G>C
NM_006514.3:c.3228+222G>C	NP_006505.3:n.3228+222G>C
XM_005265371.2:c.3237+222G>C	XP_005265428.1:n.3237+222G>C
XM_011533993.1:c.3234+222G>C	XP_011532295.1:n.3234+222G>C
XM_011533994.1:c.2943+222G>C	XP_011532296.1:n.2943+222G>C
XM_005265371.3:c.3237+222G>C	XP_005265428.1:n.3237+222G>C
XM_011533993.2:c.3234+222G>C	XP_011532295.1:n.3234+222G>C
XM_011533994.2:c.2943+222G>C	XP_011532296.1:n.2943+222G>C
NM_006514.4:c.3228+222G>C MANE Select	NP_006505.4:n.3228+222G>C