Canonical Allele Identifier: CA1358639954

Gene: SCN10A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38723910C= , CM000665.2:g.38723910C=	GRCh38
NC_000003.11:g.38765401C= , CM000665.1:g.38765401C=	GRCh37
NC_000003.10:g.38740405C=	NCBI36
NG_031891.2:g.75101G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000449082.3:c.3229-357G= MANE Select	ENSP00000390600.2:n.3229-357G=
ENST00000643924.1:c.3226-357G=	ENSP00000495595.1:n.3226-357G=
ENST00000655275.1:c.3253-357G=	ENSP00000499510.1:n.3253-357G=
ENST00000449082.2:c.3229-357G=	ENSP00000390600.2:n.3229-357G=
NM_001293306.2:c.3226-357G=	NP_001280235.2:n.3226-357G=
NM_001293307.2:c.2935-357G=	NP_001280236.2:n.2935-357G=
NM_006514.3:c.3229-357G=	NP_006505.3:n.3229-357G=
XM_005265371.2:c.3238-357G=	XP_005265428.1:n.3238-357G=
XM_011533993.1:c.3235-357G=	XP_011532295.1:n.3235-357G=
XM_011533994.1:c.2944-357G=	XP_011532296.1:n.2944-357G=
XM_005265371.3:c.3238-357G=	XP_005265428.1:n.3238-357G=
XM_011533993.2:c.3235-357G=	XP_011532295.1:n.3235-357G=
XM_011533994.2:c.2944-357G=	XP_011532296.1:n.2944-357G=
NM_006514.4:c.3229-357G= MANE Select	NP_006505.4:n.3229-357G=