Canonical Allele Identifier: CA339105612
Gene: SELENON HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.25800232T>G
GRCh37 chr1:g.26126723T>G
Revel Score:
ENST00000361547 (MANE Select) 0.527
ENST00000354177 0.527
ENST00000374315 0.527
ClinVar RCV:
RCV000541651
ClinVar Variation:
461632
dbSNP:
1174570887
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25800232T>G , CM000663.2:g.25800232T>G GRCh38
NC_000001.10:g.26126723T>G , CM000663.1:g.26126723T>G GRCh37
NC_000001.9:g.25999310T>G NCBI36
NG_009930.1:g.5057T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000354177.9:c.2T>G ENSP00000346109.5:p.Met1Arg
ENST00000494537.2:c.2T>G ENSP00000508308.1:p.Met1Arg
ENST00000361547.7:c.2T>G MANE Select ENSP00000355141.2:p.Met1Arg
ENST00000354177.8:c.2T>G ENSP00000346109.4:p.Met1Arg
ENST00000361547.6:c.2T>G ENSP00000355141.2:p.Met1Arg
ENST00000374315.1:c.2T>G ENSP00000363434.1:p.Met1Arg
NM_020451.2:c.2T>G NP_065184.2:p.Met1Arg
NM_206926.1:c.2T>G NP_996809.1:p.Met1Arg
NM_020451.3:c.2T>G MANE Select NP_065184.2:p.Met1Arg
NM_206926.2:c.2T>G NP_996809.1:p.Met1Arg
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