Canonical Allele Identifier: CA542278628

Gene: SCN10A

Linked Data

• dbSNP Id: rs1373601919
• gnomAD v2: 3-38764902-C-G
• gnomAD v4: 3-38723411-C-G
• MyVariant Identifiers: chr3:g.38764902C>G (hg19) ; chr3:g.38723411C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38723411C>G , CM000665.2:g.38723411C>G	GRCh38
NC_000003.11:g.38764902C>G , CM000665.1:g.38764902C>G	GRCh37
NC_000003.10:g.38739906C>G	NCBI36
NG_031891.2:g.75600G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000449082.3:c.3352+19G>C MANE Select	ENSP00000390600.2:n.3352+19G>C
ENST00000643924.1:c.3349+19G>C	ENSP00000495595.1:n.3349+19G>C
ENST00000655275.1:c.3376+19G>C	ENSP00000499510.1:n.3376+19G>C
ENST00000449082.2:c.3352+19G>C	ENSP00000390600.2:n.3352+19G>C
NM_001293306.2:c.3349+19G>C	NP_001280235.2:n.3349+19G>C
NM_001293307.2:c.3058+19G>C	NP_001280236.2:n.3058+19G>C
NM_006514.3:c.3352+19G>C	NP_006505.3:n.3352+19G>C
XM_005265371.2:c.3361+19G>C	XP_005265428.1:n.3361+19G>C
XM_011533993.1:c.3358+19G>C	XP_011532295.1:n.3358+19G>C
XM_011533994.1:c.3067+19G>C	XP_011532296.1:n.3067+19G>C
XM_005265371.3:c.3361+19G>C	XP_005265428.1:n.3361+19G>C
XM_011533993.2:c.3358+19G>C	XP_011532295.1:n.3358+19G>C
XM_011533994.2:c.3067+19G>C	XP_011532296.1:n.3067+19G>C
NM_006514.4:c.3352+19G>C MANE Select	NP_006505.4:n.3352+19G>C