Canonical Allele Identifier: CA19698368
Gene: SELENON HGNC NCBI

Linked Data

dbSNP Id: rs760108862
gnomAD v2: 1-26135510-C-A
gnomAD v4: 1-25809019-C-A
MyVariant Identifiers: chr1:g.26135510C>A (hg19) chr1:g.25809019C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25809019C>A , CM000663.2:g.25809019C>A GRCh38
NC_000001.10:g.26135510C>A , CM000663.1:g.26135510C>A GRCh37
NC_000001.9:g.26008097C>A NCBI36
NG_009930.1:g.13844C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000354177.9:c.646-76C>A ENSP00000346109.5:n.646-76C>A
ENST00000494537.2:c.646-7C>A ENSP00000508308.1:n.646-7C>A
ENST00000361547.7:c.748-7C>A MANE Select ENSP00000355141.2:n.748-7C>A
ENST00000354177.8:c.646-7C>A ENSP00000346109.4:n.646-7C>A
ENST00000361547.6:c.748-7C>A ENSP00000355141.2:n.748-7C>A
ENST00000374315.1:c.646-7C>A ENSP00000363434.1:n.646-7C>A
NM_020451.2:c.748-7C>A NP_065184.2:n.748-7C>A
NM_206926.1:c.646-7C>A NP_996809.1:n.646-7C>A
NM_020451.3:c.748-7C>A MANE Select NP_065184.2:n.748-7C>A
NM_206926.2:c.646-7C>A NP_996809.1:n.646-7C>A
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