Canonical Allele Identifier: CA339105610

Gene: SELENON

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25800232T>C , CM000663.2:g.25800232T>C	GRCh38
NC_000001.10:g.26126723T>C , CM000663.1:g.26126723T>C	GRCh37
NC_000001.9:g.25999310T>C	NCBI36
NG_009930.1:g.5057T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.2T>C	ENSP00000346109.5:p.Met1Thr
ENST00000494537.2:c.2T>C	ENSP00000508308.1:p.Met1Thr
ENST00000361547.7:c.2T>C MANE Select	ENSP00000355141.2:p.Met1Thr
ENST00000354177.8:c.2T>C	ENSP00000346109.4:p.Met1Thr
ENST00000361547.6:c.2T>C	ENSP00000355141.2:p.Met1Thr
ENST00000374315.1:c.2T>C	ENSP00000363434.1:p.Met1Thr
NM_020451.2:c.2T>C	NP_065184.2:p.Met1Thr
NM_206926.1:c.2T>C	NP_996809.1:p.Met1Thr
NM_020451.3:c.2T>C MANE Select	NP_065184.2:p.Met1Thr
NM_206926.2:c.2T>C	NP_996809.1:p.Met1Thr