Canonical Allele Identifier: CA352156717

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38766736A>C (hg19) ; chr3:g.38725245A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725245A>C , CM000665.2:g.38725245A>C	GRCh38
NC_000003.11:g.38766736A>C , CM000665.1:g.38766736A>C	GRCh37
NC_000003.10:g.38741740A>C	NCBI36
NG_031891.2:g.73766T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3157T>G MANE Select	ENSP00000390600.2:p.Ser1053Ala
ENST00000643924.1:c.3154T>G	ENSP00000495595.1:p.Ser1052Ala
ENST00000655275.1:c.3181T>G	ENSP00000499510.1:p.Ser1061Ala
ENST00000449082.2:c.3157T>G	ENSP00000390600.2:p.Ser1053Ala
NM_001293306.2:c.3154T>G	NP_001280235.2:p.Ser1052Ala
NM_001293307.2:c.2863T>G	NP_001280236.2:p.Ser955Ala
NM_006514.3:c.3157T>G	NP_006505.3:p.Ser1053Ala
XM_005265371.2:c.3166T>G	XP_005265428.1:p.Ser1056Ala
XM_011533993.1:c.3163T>G	XP_011532295.1:p.Ser1055Ala
XM_011533994.1:c.2872T>G	XP_011532296.1:p.Ser958Ala
XM_005265371.3:c.3166T>G	XP_005265428.1:p.Ser1056Ala
XM_011533993.2:c.3163T>G	XP_011532295.1:p.Ser1055Ala
XM_011533994.2:c.2872T>G	XP_011532296.1:p.Ser958Ala
NM_006514.4:c.3157T>G MANE Select	NP_006505.4:p.Ser1053Ala