Canonical Allele Identifier: CA1358640606

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725304A= , CM000665.2:g.38725304A=	GRCh38
NC_000003.11:g.38766795A= , CM000665.1:g.38766795A=	GRCh37
NC_000003.10:g.38741799A=	NCBI36
NG_031891.2:g.73707T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3098T= MANE Select	ENSP00000390600.2:p.Leu1033=
ENST00000643924.1:c.3095T=	ENSP00000495595.1:p.Leu1032=
ENST00000655275.1:c.3122T=	ENSP00000499510.1:p.Leu1041=
ENST00000449082.2:c.3098T=	ENSP00000390600.2:p.Leu1033=
NM_001293306.2:c.3095T=	NP_001280235.2:p.Leu1032=
NM_001293307.2:c.2804T=	NP_001280236.2:p.Leu935=
NM_006514.3:c.3098T=	NP_006505.3:p.Leu1033=
XM_005265371.2:c.3107T=	XP_005265428.1:p.Leu1036=
XM_011533993.1:c.3104T=	XP_011532295.1:p.Leu1035=
XM_011533994.1:c.2813T=	XP_011532296.1:p.Leu938=
XM_005265371.3:c.3107T=	XP_005265428.1:p.Leu1036=
XM_011533993.2:c.3104T=	XP_011532295.1:p.Leu1035=
XM_011533994.2:c.2813T=	XP_011532296.1:p.Leu938=
NM_006514.4:c.3098T= MANE Select	NP_006505.4:p.Leu1033=