Canonical Allele Identifier: CA433138562

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38766785G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725294G>C , CM000665.2:g.38725294G>C	GRCh38
NC_000003.11:g.38766785G>C , CM000665.1:g.38766785G>C	GRCh37
NC_000003.10:g.38741789G>C	NCBI36
NG_031891.2:g.73717C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3108C>G MANE Select	ENSP00000390600.2:p.Val1036=
ENST00000643924.1:c.3105C>G	ENSP00000495595.1:p.Val1035=
ENST00000655275.1:c.3132C>G	ENSP00000499510.1:p.Val1044=
ENST00000449082.2:c.3108C>G	ENSP00000390600.2:p.Val1036=
NM_001293306.2:c.3105C>G	NP_001280235.2:p.Val1035=
NM_001293307.2:c.2814C>G	NP_001280236.2:p.Val938=
NM_006514.3:c.3108C>G	NP_006505.3:p.Val1036=
XM_005265371.2:c.3117C>G	XP_005265428.1:p.Val1039=
XM_011533993.1:c.3114C>G	XP_011532295.1:p.Val1038=
XM_011533994.1:c.2823C>G	XP_011532296.1:p.Val941=
XM_005265371.3:c.3117C>G	XP_005265428.1:p.Val1039=
XM_011533993.2:c.3114C>G	XP_011532295.1:p.Val1038=
XM_011533994.2:c.2823C>G	XP_011532296.1:p.Val941=
NM_006514.4:c.3108C>G MANE Select	NP_006505.4:p.Val1036=