Canonical Allele Identifier: CA696609
Gene: SELENON HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.25808774G>A
GRCh37 chr1:g.26135265G>A
gnomAD v2:
1:26135265 G / A
gnomAD v3:
1:25808774 G / A
gnomAD v4:
chr1-25808774-G-A
Joint Max Group AF 0.00015372 (SAS)
Genomes Max Group AF 0.00007279 (SAS)
Exomes Max Group AF 0.00014346 (SAS)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25808774G>A , CM000663.2:g.25808774G>A GRCh38
NC_000001.10:g.26135265G>A , CM000663.1:g.26135265G>A GRCh37
NC_000001.9:g.26007852G>A NCBI36
NG_009930.1:g.13599G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354177.9:c.630G>A ENSP00000346109.5:p.Pro210=
ENST00000494537.2:c.630G>A ENSP00000508308.1:p.Pro210=
ENST00000361547.7:c.732G>A MANE Select ENSP00000355141.2:p.Pro244=
ENST00000354177.8:c.630G>A ENSP00000346109.4:p.Pro210=
ENST00000361547.6:c.732G>A ENSP00000355141.2:p.Pro244=
ENST00000374315.1:c.630G>A ENSP00000363434.1:p.Pro210=
NM_020451.2:c.732G>A NP_065184.2:p.Pro244=
NM_206926.1:c.630G>A NP_996809.1:p.Pro210=
NM_020451.3:c.732G>A MANE Select NP_065184.2:p.Pro244=
NM_206926.2:c.630G>A NP_996809.1:p.Pro210=
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