Canonical Allele Identifier: CA433138567

Gene: SCN10A

Linked Data

• gnomAD v4: 3-38725297-T-C
• MyVariant Identifiers: chr3:g.38766788T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38725297T>C , CM000665.2:g.38725297T>C	GRCh38
NC_000003.11:g.38766788T>C , CM000665.1:g.38766788T>C	GRCh37
NC_000003.10:g.38741792T>C	NCBI36
NG_031891.2:g.73714A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449082.3:c.3105A>G MANE Select	ENSP00000390600.2:p.Gln1035=
ENST00000643924.1:c.3102A>G	ENSP00000495595.1:p.Gln1034=
ENST00000655275.1:c.3129A>G	ENSP00000499510.1:p.Gln1043=
ENST00000449082.2:c.3105A>G	ENSP00000390600.2:p.Gln1035=
NM_001293306.2:c.3102A>G	NP_001280235.2:p.Gln1034=
NM_001293307.2:c.2811A>G	NP_001280236.2:p.Gln937=
NM_006514.3:c.3105A>G	NP_006505.3:p.Gln1035=
XM_005265371.2:c.3114A>G	XP_005265428.1:p.Gln1038=
XM_011533993.1:c.3111A>G	XP_011532295.1:p.Gln1037=
XM_011533994.1:c.2820A>G	XP_011532296.1:p.Gln940=
XM_005265371.3:c.3114A>G	XP_005265428.1:p.Gln1038=
XM_011533993.2:c.3111A>G	XP_011532295.1:p.Gln1037=
XM_011533994.2:c.2820A>G	XP_011532296.1:p.Gln940=
NM_006514.4:c.3105A>G MANE Select	NP_006505.4:p.Gln1035=