Canonical Allele Identifier: CA2644200967
Gene: SELENON HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25812564_25812603del , CM000663.2:g.25812564_25812603del GRCh38
NC_000001.10:g.26139055_26139094del , CM000663.1:g.26139055_26139094del GRCh37
NC_000001.9:g.26011642_26011681del NCBI36
NG_009930.1:g.17389_17428del

Transcript Alleles

HGVS Amino-acid Change
ENST00000354177.9:c.1111-123_1111-84del ENSP00000346109.5:n.1111-123_1111-84del
ENST00000494537.2:c.1180-123_1180-84del ENSP00000508308.1:n.1180-123_1180-84del
ENST00000361547.7:c.1282-123_1282-84del MANE Select ENSP00000355141.2:n.1282-123_1282-84del
ENST00000354177.8:c.1180-123_1180-84del ENSP00000346109.4:n.1180-123_1180-84del
ENST00000361547.6:c.1282-123_1282-84del ENSP00000355141.2:n.1282-123_1282-84del
ENST00000374315.1:c.1180-123_1180-84del ENSP00000363434.1:n.1180-123_1180-84del
ENST00000559265.1:n.255+685_255+724del
NM_020451.2:c.1282-123_1282-84del NP_065184.2:n.1282-123_1282-84del
NM_206926.1:c.1180-123_1180-84del NP_996809.1:n.1180-123_1180-84del
NM_020451.3:c.1282-123_1282-84del MANE Select NP_065184.2:n.1282-123_1282-84del
NM_206926.2:c.1180-123_1180-84del NP_996809.1:n.1180-123_1180-84del