Canonical Allele Identifier: CA1358640570

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725226G= , CM000665.2:g.38725226G=	GRCh38
NC_000003.11:g.38766717G= , CM000665.1:g.38766717G=	GRCh37
NC_000003.10:g.38741721G=	NCBI36
NG_031891.2:g.73785C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3176C= MANE Select	ENSP00000390600.2:p.Pro1059=
ENST00000643924.1:c.3173C=	ENSP00000495595.1:p.Pro1058=
ENST00000655275.1:c.3200C=	ENSP00000499510.1:p.Pro1067=
ENST00000449082.2:c.3176C=	ENSP00000390600.2:p.Pro1059=
NM_001293306.2:c.3173C=	NP_001280235.2:p.Pro1058=
NM_001293307.2:c.2882C=	NP_001280236.2:p.Pro961=
NM_006514.3:c.3176C=	NP_006505.3:p.Pro1059=
XM_005265371.2:c.3185C=	XP_005265428.1:p.Pro1062=
XM_011533993.1:c.3182C=	XP_011532295.1:p.Pro1061=
XM_011533994.1:c.2891C=	XP_011532296.1:p.Pro964=
XM_005265371.3:c.3185C=	XP_005265428.1:p.Pro1062=
XM_011533993.2:c.3182C=	XP_011532295.1:p.Pro1061=
XM_011533994.2:c.2891C=	XP_011532296.1:p.Pro964=
NM_006514.4:c.3176C= MANE Select	NP_006505.4:p.Pro1059=