Canonical Allele Identifier: CA352156841

Gene: SCN10A

Linked Data

• MyVariant Identifiers: chr3:g.38766796G>T (hg19) ; chr3:g.38725305G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725305G>T , CM000665.2:g.38725305G>T	GRCh38
NC_000003.11:g.38766796G>T , CM000665.1:g.38766796G>T	GRCh37
NC_000003.10:g.38741800G>T	NCBI36
NG_031891.2:g.73706C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3097C>A MANE Select	ENSP00000390600.2:p.Leu1033Met
ENST00000643924.1:c.3094C>A	ENSP00000495595.1:p.Leu1032Met
ENST00000655275.1:c.3121C>A	ENSP00000499510.1:p.Leu1041Met
ENST00000449082.2:c.3097C>A	ENSP00000390600.2:p.Leu1033Met
NM_001293306.2:c.3094C>A	NP_001280235.2:p.Leu1032Met
NM_001293307.2:c.2803C>A	NP_001280236.2:p.Leu935Met
NM_006514.3:c.3097C>A	NP_006505.3:p.Leu1033Met
XM_005265371.2:c.3106C>A	XP_005265428.1:p.Leu1036Met
XM_011533993.1:c.3103C>A	XP_011532295.1:p.Leu1035Met
XM_011533994.1:c.2812C>A	XP_011532296.1:p.Leu938Met
XM_005265371.3:c.3106C>A	XP_005265428.1:p.Leu1036Met
XM_011533993.2:c.3103C>A	XP_011532295.1:p.Leu1035Met
XM_011533994.2:c.2812C>A	XP_011532296.1:p.Leu938Met
NM_006514.4:c.3097C>A MANE Select	NP_006505.4:p.Leu1033Met