Canonical Allele Identifier: CA352167797
Gene: SCN10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.38752509A>T , CM000665.2:g.38752509A>T GRCh38
NC_000003.11:g.38794000A>T , CM000665.1:g.38794000A>T GRCh37
NC_000003.10:g.38769004A>T NCBI36
NG_031891.2:g.46502T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000449082.3:c.1465T>A MANE Select ENSP00000390600.2:p.Phe489Ile
ENST00000643924.1:c.1465T>A ENSP00000495595.1:p.Phe489Ile
ENST00000655275.1:c.1492T>A ENSP00000499510.1:p.Phe498Ile
ENST00000449082.2:c.1465T>A ENSP00000390600.2:p.Phe489Ile
NM_001293306.2:c.1465T>A NP_001280235.2:p.Phe489Ile
NM_001293307.2:c.1462-2325T>A NP_001280236.2:n.1462-2325T>A
NM_006514.3:c.1465T>A NP_006505.3:p.Phe489Ile
XM_005265371.2:c.1474T>A XP_005265428.1:p.Phe492Ile
XM_011533993.1:c.1474T>A XP_011532295.1:p.Phe492Ile
XM_011533994.1:c.1471-2325T>A XP_011532296.1:n.1471-2325T>A
XM_005265371.3:c.1474T>A XP_005265428.1:p.Phe492Ile
XM_011533993.2:c.1474T>A XP_011532295.1:p.Phe492Ile
XM_011533994.2:c.1471-2325T>A XP_011532296.1:n.1471-2325T>A
NM_006514.4:c.1465T>A MANE Select NP_006505.4:p.Phe489Ile