Canonical Allele Identifier: CA1159807798
Gene: SELENON HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25812597_25812609delinsACACACACACTTG , CM000663.2:g.25812597_25812609delinsACACACACACTTG GRCh38
NC_000001.10:g.26139088_26139100delinsACACACACACTTG , CM000663.1:g.26139088_26139100delinsACACACACACTTG GRCh37
NC_000001.9:g.26011675_26011687delinsACACACACACTTG NCBI36
NG_009930.1:g.17422_17434delinsACACACACACTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000354177.9:c.1111-90_1111-78delinsACACACACACTTG ENSP00000346109.5:n.1111-90_1111-78delinsACACACACACTTG
ENST00000494537.2:c.1180-90_1180-78delinsACACACACACTTG ENSP00000508308.1:n.1180-90_1180-78delinsACACACACACTTG
ENST00000361547.7:c.1282-90_1282-78delinsACACACACACTTG MANE Select ENSP00000355141.2:n.1282-90_1282-78delinsACACACACACTTG
ENST00000354177.8:c.1180-90_1180-78delinsACACACACACTTG ENSP00000346109.4:n.1180-90_1180-78delinsACACACACACTTG
ENST00000361547.6:c.1282-90_1282-78delinsACACACACACTTG ENSP00000355141.2:n.1282-90_1282-78delinsACACACACACTTG
ENST00000374315.1:c.1180-90_1180-78delinsACACACACACTTG ENSP00000363434.1:n.1180-90_1180-78delinsACACACACACTTG
ENST00000559265.1:n.255+718_255+730delinsACACACACACTTG
NM_020451.2:c.1282-90_1282-78delinsACACACACACTTG NP_065184.2:n.1282-90_1282-78delinsACACACACACTTG
NM_206926.1:c.1180-90_1180-78delinsACACACACACTTG NP_996809.1:n.1180-90_1180-78delinsACACACACACTTG
NM_020451.3:c.1282-90_1282-78delinsACACACACACTTG MANE Select NP_065184.2:n.1282-90_1282-78delinsACACACACACTTG
NM_206926.2:c.1180-90_1180-78delinsACACACACACTTG NP_996809.1:n.1180-90_1180-78delinsACACACACACTTG