Canonical Allele Identifier: CA2644201035

Gene: SELENON

Linked Data

• gnomAD v4: 1-25812595-ACACACACACACTTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812603_25812616del , CM000663.2:g.25812603_25812616del	GRCh38
NC_000001.10:g.26139094_26139107del , CM000663.1:g.26139094_26139107del	GRCh37
NC_000001.9:g.26011681_26011694del	NCBI36
NG_009930.1:g.17428_17441del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1111-84_1111-71del	ENSP00000346109.5:n.1111-84_1111-71del
ENST00000494537.2:c.1180-84_1180-71del	ENSP00000508308.1:n.1180-84_1180-71del
ENST00000361547.7:c.1282-84_1282-71del MANE Select	ENSP00000355141.2:n.1282-84_1282-71del
ENST00000354177.8:c.1180-84_1180-71del	ENSP00000346109.4:n.1180-84_1180-71del
ENST00000361547.6:c.1282-84_1282-71del	ENSP00000355141.2:n.1282-84_1282-71del
ENST00000374315.1:c.1180-84_1180-71del	ENSP00000363434.1:n.1180-84_1180-71del
ENST00000559265.1:n.255+724_255+737del
NM_020451.2:c.1282-84_1282-71del	NP_065184.2:n.1282-84_1282-71del
NM_206926.1:c.1180-84_1180-71del	NP_996809.1:n.1180-84_1180-71del
NM_020451.3:c.1282-84_1282-71del MANE Select	NP_065184.2:n.1282-84_1282-71del
NM_206926.2:c.1180-84_1180-71del	NP_996809.1:n.1180-84_1180-71del