Canonical Allele Identifier: CA352155955

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38764919A>G (hg19) ; chr3:g.38723428A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38723428A>G , CM000665.2:g.38723428A>G	GRCh38
NC_000003.11:g.38764919A>G , CM000665.1:g.38764919A>G	GRCh37
NC_000003.10:g.38739923A>G	NCBI36
NG_031891.2:g.75583T>C

Transcript Alleles

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