Canonical Allele Identifier: CA1159806231
Gene: SELENON HGNC NCBI

Linked Data

dbSNP Id: rs2047937796
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25809298T>C , CM000663.2:g.25809298T>C GRCh38
NC_000001.10:g.26135789T>C , CM000663.1:g.26135789T>C GRCh37
NC_000001.9:g.26008376T>C NCBI36
NG_009930.1:g.14123T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000354177.9:c.701+148T>C ENSP00000346109.5:n.701+148T>C
ENST00000494537.2:c.770+148T>C ENSP00000508308.1:n.770+148T>C
ENST00000361547.7:c.872+148T>C MANE Select ENSP00000355141.2:n.872+148T>C
ENST00000354177.8:c.770+148T>C ENSP00000346109.4:n.770+148T>C
ENST00000361547.6:c.872+148T>C ENSP00000355141.2:n.872+148T>C
ENST00000374315.1:c.770+148T>C ENSP00000363434.1:n.770+148T>C
NM_020451.2:c.872+148T>C NP_065184.2:n.872+148T>C
NM_206926.1:c.770+148T>C NP_996809.1:n.770+148T>C
NM_020451.3:c.872+148T>C MANE Select NP_065184.2:n.872+148T>C
NM_206926.2:c.770+148T>C NP_996809.1:n.770+148T>C
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