Canonical Allele Identifier: CA352156679

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38766717G>C (hg19) ; chr3:g.38725226G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725226G>C , CM000665.2:g.38725226G>C	GRCh38
NC_000003.11:g.38766717G>C , CM000665.1:g.38766717G>C	GRCh37
NC_000003.10:g.38741721G>C	NCBI36
NG_031891.2:g.73785C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3176C>G MANE Select	ENSP00000390600.2:p.Pro1059Arg
ENST00000643924.1:c.3173C>G	ENSP00000495595.1:p.Pro1058Arg
ENST00000655275.1:c.3200C>G	ENSP00000499510.1:p.Pro1067Arg
ENST00000449082.2:c.3176C>G	ENSP00000390600.2:p.Pro1059Arg
NM_001293306.2:c.3173C>G	NP_001280235.2:p.Pro1058Arg
NM_001293307.2:c.2882C>G	NP_001280236.2:p.Pro961Arg
NM_006514.3:c.3176C>G	NP_006505.3:p.Pro1059Arg
XM_005265371.2:c.3185C>G	XP_005265428.1:p.Pro1062Arg
XM_011533993.1:c.3182C>G	XP_011532295.1:p.Pro1061Arg
XM_011533994.1:c.2891C>G	XP_011532296.1:p.Pro964Arg
XM_005265371.3:c.3185C>G	XP_005265428.1:p.Pro1062Arg
XM_011533993.2:c.3182C>G	XP_011532295.1:p.Pro1061Arg
XM_011533994.2:c.2891C>G	XP_011532296.1:p.Pro964Arg
NM_006514.4:c.3176C>G MANE Select	NP_006505.4:p.Pro1059Arg