Canonical Allele Identifier: CA352156683

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38766718G>T (hg19) ; chr3:g.38725227G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725227G>T , CM000665.2:g.38725227G>T	GRCh38
NC_000003.11:g.38766718G>T , CM000665.1:g.38766718G>T	GRCh37
NC_000003.10:g.38741722G>T	NCBI36
NG_031891.2:g.73784C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3175C>A MANE Select	ENSP00000390600.2:p.Pro1059Thr
ENST00000643924.1:c.3172C>A	ENSP00000495595.1:p.Pro1058Thr
ENST00000655275.1:c.3199C>A	ENSP00000499510.1:p.Pro1067Thr
ENST00000449082.2:c.3175C>A	ENSP00000390600.2:p.Pro1059Thr
NM_001293306.2:c.3172C>A	NP_001280235.2:p.Pro1058Thr
NM_001293307.2:c.2881C>A	NP_001280236.2:p.Pro961Thr
NM_006514.3:c.3175C>A	NP_006505.3:p.Pro1059Thr
XM_005265371.2:c.3184C>A	XP_005265428.1:p.Pro1062Thr
XM_011533993.1:c.3181C>A	XP_011532295.1:p.Pro1061Thr
XM_011533994.1:c.2890C>A	XP_011532296.1:p.Pro964Thr
XM_005265371.3:c.3184C>A	XP_005265428.1:p.Pro1062Thr
XM_011533993.2:c.3181C>A	XP_011532295.1:p.Pro1061Thr
XM_011533994.2:c.2890C>A	XP_011532296.1:p.Pro964Thr
NM_006514.4:c.3175C>A MANE Select	NP_006505.4:p.Pro1059Thr