Canonical Allele Identifier: CA2639311622
Gene: SCN4A HGNC NCBI

Linked Data

gnomAD v4: 17-63972098-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63972098T>A , CM000679.2:g.63972098T>A GRCh38
NC_000017.10:g.62049458T>A , CM000679.1:g.62049458T>A GRCh37
NC_000017.9:g.59403190T>A NCBI36
NG_011699.1:g.5821A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.482+38A>T MANE Select ENSP00000396320.1:n.482+38A>T
ENST00000578147.5:c.482+38A>T ENSP00000463963.1:n.482+38A>T
NM_000334.4:c.482+38A>T MANE Select NP_000325.4:n.482+38A>T
XM_005257566.3:c.482+38A>T XP_005257623.1:n.482+38A>T
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