Canonical Allele Identifier: CA341956916

Gene: SELENBP1

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151365568C>A , CM000663.2:g.151365568C>A	GRCh38
NC_000001.10:g.151338044C>A , CM000663.1:g.151338044C>A	GRCh37
NC_000001.9:g.149604668C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368868.10:c.1039G>T MANE Select	ENSP00000357861.5:p.Gly347Ter
ENST00000368868.9:c.1039G>T	ENSP00000357861.5:p.Gly347Ter
ENST00000423070.5:c.*671G>T	ENSP00000416206.1:n.*671G>T
ENST00000426705.6:c.1165G>T	ENSP00000397261.2:p.Gly389Ter
ENST00000427977.6:c.*633+38G>T	ENSP00000412816.1:n.*633+38G>T
ENST00000443708.5:c.*671G>T	ENSP00000402531.1:n.*671G>T
ENST00000447402.7:c.853G>T	ENSP00000413960.3:p.Gly285Ter
ENST00000455397.5:c.*488G>T	ENSP00000395637.1:n.*488G>T
ENST00000463664.5:n.1344G>T
ENST00000470345.5:n.1514G>T
ENST00000474352.5:n.1941G>T
ENST00000493560.5:n.1344G>T
NM_001258288.1:c.853G>T	NP_001245217.1:p.Gly285Ter
NM_001258289.1:c.1165G>T	NP_001245218.1:p.Gly389Ter
NM_003944.3:c.1039G>T	NP_003935.2:p.Gly347Ter
XM_011510110.1:c.1165G>T	XP_011508412.1:p.Gly389Ter
XM_011510111.1:c.445G>T	XP_011508413.1:p.Gly149Ter
XR_921993.1:n.1149G>T
XM_024450671.1:c.445G>T	XP_024306439.1:p.Gly149Ter
XR_002957987.1:n.1313G>T
XR_921993.2:n.1141G>T
NM_003944.4:c.1039G>T MANE Select	NP_003935.2:p.Gly347Ter
NM_001258288.2:c.853G>T	NP_001245217.1:p.Gly285Ter
NM_001258289.2:c.1165G>T	NP_001245218.1:p.Gly389Ter