Canonical Allele Identifier: CA352156796

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38766776A>C (hg19) ; chr3:g.38725285A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725285A>C , CM000665.2:g.38725285A>C	GRCh38
NC_000003.11:g.38766776A>C , CM000665.1:g.38766776A>C	GRCh37
NC_000003.10:g.38741780A>C	NCBI36
NG_031891.2:g.73726T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3117T>G MANE Select	ENSP00000390600.2:p.Cys1039Trp
ENST00000643924.1:c.3114T>G	ENSP00000495595.1:p.Cys1038Trp
ENST00000655275.1:c.3141T>G	ENSP00000499510.1:p.Cys1047Trp
ENST00000449082.2:c.3117T>G	ENSP00000390600.2:p.Cys1039Trp
NM_001293306.2:c.3114T>G	NP_001280235.2:p.Cys1038Trp
NM_001293307.2:c.2823T>G	NP_001280236.2:p.Cys941Trp
NM_006514.3:c.3117T>G	NP_006505.3:p.Cys1039Trp
XM_005265371.2:c.3126T>G	XP_005265428.1:p.Cys1042Trp
XM_011533993.1:c.3123T>G	XP_011532295.1:p.Cys1041Trp
XM_011533994.1:c.2832T>G	XP_011532296.1:p.Cys944Trp
XM_005265371.3:c.3126T>G	XP_005265428.1:p.Cys1042Trp
XM_011533993.2:c.3123T>G	XP_011532295.1:p.Cys1041Trp
XM_011533994.2:c.2832T>G	XP_011532296.1:p.Cys944Trp
NM_006514.4:c.3117T>G MANE Select	NP_006505.4:p.Cys1039Trp