Canonical Allele Identifier: CA2644201054

Gene: SELENON

Linked Data

• gnomAD v4: 1-25812605-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812606_25812607del , CM000663.2:g.25812606_25812607del	GRCh38
NC_000001.10:g.26139097_26139098del , CM000663.1:g.26139097_26139098del	GRCh37
NC_000001.9:g.26011684_26011685del	NCBI36
NG_009930.1:g.17431_17432del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1111-81_1111-80del	ENSP00000346109.5:n.1111-81_1111-80del
ENST00000494537.2:c.1180-81_1180-80del	ENSP00000508308.1:n.1180-81_1180-80del
ENST00000361547.7:c.1282-81_1282-80del MANE Select	ENSP00000355141.2:n.1282-81_1282-80del
ENST00000354177.8:c.1180-81_1180-80del	ENSP00000346109.4:n.1180-81_1180-80del
ENST00000361547.6:c.1282-81_1282-80del	ENSP00000355141.2:n.1282-81_1282-80del
ENST00000374315.1:c.1180-81_1180-80del	ENSP00000363434.1:n.1180-81_1180-80del
ENST00000559265.1:n.255+727_255+728del
NM_020451.2:c.1282-81_1282-80del	NP_065184.2:n.1282-81_1282-80del
NM_206926.1:c.1180-81_1180-80del	NP_996809.1:n.1180-81_1180-80del
NM_020451.3:c.1282-81_1282-80del MANE Select	NP_065184.2:n.1282-81_1282-80del
NM_206926.2:c.1180-81_1180-80del	NP_996809.1:n.1180-81_1180-80del